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  • Ewing's Sarcoma Wikipedia
    PMID 29431183 . ^ Lahl M, Fisher VL, Laschinger K (February 2008). "Ewing's sarcoma family of tumors: an overview from diagnosis to survivorship".
    EWSR1, FLI1, EGR2, ERG, ETV1, ETV4, STAG2, CIZ1, NF1, BRD4, DUX4, FLII, NUTM1, TP53, CXCR4, BAP1, RB1, C1orf127, PARP1, RPL24P2, CCND1, SRP14-AS1, FUS, IGF1R, CDKN2A, CD99, CIC, IGF1, BCOR, VEGFA, PIK3CA, PIK3CD, CDK4, PIK3CB, EZH2, PIK3CG, NR0B1, CCNB3, FEV, ATF1, FOXO1, SMUG1, TNFSF10, NFATC2, HLA-A, MYC, TAF15, HIF1A, COL11A2, CAV1, KDM1A, BMI1, CNMD, AKT1, WT1, CCK, PAX3, TNF, KDM3A, STEAP1, MBD2, MDM2, BCL2, COMMD3-BMI1, EWSAT1, ERBB2, ELAVL2, EPHA2, PTEN, ABCB1, ROCK1, DNER, IFNB1, XAGE1A, TNC, FGF2, SH2D1B, HOXD@, XAGE1B, CASP8, LIF, ALK, TGFBR2, STAT3, CTLA4, VIM, SOX2, DDIT3, PAX7, MMP1, MAPK1, MEN1, NKX2-2, NGF, BCL11B, HLA-DOA, MMP9, MET, HGF, RASSF2, NAMPT, TARDBP, NOTCH1, KMT2A, HES1, GLI1, EMG1, DTL, IL2, PDCD1, PDGFRB, PAPPA, IGFBP3, NES, TWIST1, NTRK1, PLK1, RASSF1, CCN3, HTC2, LDHA, NPY, IGF2BP3, PHGDH, MAML3, PTPRC, FAS, ETV5, BCR, FOXM1, TERT, RHD, SMARCB1, S100A1, BRCA1, CSF3, ETS1, EGFR, S100B, CHEK1, ERBB4, ZYX, ENG, TGFB1, E2F3, AURKB, MIR34A, MALAT1, EZR, PTPN13, CBL, CD38, ROCK2, CCND2, FOLH1, CD34, TNFRSF10A, SCG2, HMGA2, REEP5, STRAP, ARID1A, MLXIP, ZBTB16, ZAP70, CHP1, EBNA1BP2, MMRN1, YWHAE, XBP1, WNT5A, MIR708, H3P28, PPRC1, SMARCA5, BCAR1, JTB, YAP1, NR1I3, TMX2-CTNND1, TRIM13, TRIB1, ADAMTS4, RABEPK, SPRY1, RAMP1, ARHGEF2, USP6, STAG1, LANCL1, OLFM1, PIK3R3, HSPB3, SNURF, NR1I2, PROM1, HDAC3, BANF1, TNFRSF10B, TP53I3, ABCC3, BECN1, TP63, USP19, EED, CDK12, TBC1D9, GSTK1, ARMH1, DLX6-AS1, CAVIN1, PGP, MIR20B, MIR193B, FNDC5, CTAG1A, POU5F1P3, LRWD1, POU5F1P4, KDM1B, MARCHF8, RHOV, ASXL1, PRIMA1, CACUL1, CXADRP1, SLCO6A1, IL31RA, BORCS5, FOXP4, PRRT2, SOX2-OT, SH2D4B, ATG4B, ERVFRD-1, MIR34B, MIR31, MIR30D, MIR30A, MIR301A, MIR29B2, MIR29B1, MIR22, MIR21, MIR199B, MIR199A2, MIR335, MIR199A1, MIR186, MIR185, MIR181C, MIR15A, MIR145, MIR139, MIR130B, MIR10B, MIR107, MIRLET7G, CEP41, FOXQ1, SLFN11, FATE1, NME1-NME2, TET2, KRT20, MIR17HG, GDE1, PHF11, PSAT1, CD274, MYLIP, SETD2, IGHV1-12, AGO2, DKK2, PHF19, MIR584, PLA2G15, SUZ12, MIR638, HEY1, SF3B1, KTWS, SATB2, FBXW11, HEATR3, ZNF331, PBK, MRPL41, DCLK3, RITA1, LINGO1, ACCS, AKT1S1, ZNF93, CD276, DHDDS, LIN28A, NKAP, SOX17, LMO3, XYLT2, ZBTB4, KIDINS220, ABHD6, CD248, CCNL1, ACKR3, CHPT1, PRMT8, ACSS2, ACTB, PTK2, TRIP6, FOXC1, GCY, GATA3, GAS6, GAB1, MTOR, FOSB, FOS, FN1, FLT4, FLT3, FHIT, GHRH, FGFR1, FGF4, FCGRT, FAP, EYA3, ERN1, ERF, EPHB2, EPHA3, EMD, GDNF, GJA1, TNNT1, HOXD11, IGF2, IFNG, IFNA13, IFNA1, HSP90AA1, HSPB2, HSPB1, HSPA4, HPRT1, HOXD13, HLA-G, GLG1, HLA-C, HLA-B, NRG1, HDGF, H2AX, GZMB, MSH6, GSTM4, NR3C1, GRB10, EGR1, EGF, EDNRB, AXL, RUNX3, RUNX2, CASR, CASP9, CASP3, CALCB, CALCA, BTK, BID, BDNF, ATR, EDNRA, SERPINC1, ARR3, ARHGAP1, ABCC6, KLK3, APOC3, XIAP, ALDH1A1, ALCAM, ADRB3, CD6, MS4A1, CD86, CD79A, E2F4, DSPP, DPP4, DDX3X, DCC, CYP2C8, CXADR, CTNND1, CTNNB1, CTAG1B, CSF1R, CSE1L, MAPK14, CRP, CEBPB, CDKN2B, CDK6, CDK2, CDH11, CDH2, CDC42, IGL, IHH, IL6, PTPN11, CCL21, S100A12, BRD2, RNF2, RET, REST, RAG2, RAC1, NECTIN2, PTPRD, PTGS2, POU5F1, PTCH1, PSPH, PSMD7, RELN, MAP2K7, MAPK8, PRKCB, PRKCA, PRKAR1A, PRF1, CXCL12, SET, SFRP5, SLC1A5, TMPRSS2, TSPAN7, TLE1, TIE1, THY1, TRBV20OR9-2, TCF4, TBX5, TARBP2, SYP, SYK, SSX1, SST, SRC, SPN, SPG7, SP1, SNRPN, SMN2, SMN1, SLC2A1, PPP1R1A, PMS2, IL9, KIT, MCF2, MCAM, LRP1, LPP, LOX, LGALS3BP, STMN1, RPSA, KRT17, KRAS, KCNA5, PMAIP1, CD82, JUND, JUNB, JUN, JAK1, INSRR, INSR, INSM1, ILK, IL15, MCL1, MDK, MEIS1, MAP3K3, PCNA, PAK3, PAK1, PAFAH1B1, OSM, ROR1, NTRK3, NPTX2, NPM1, NME2, NME1, NNAT, NF2, NCAM1, MYCN, MUC5AC, MSH2, MMP11, MME, MLH1, MGST1, H3P10
    • Ewing Sarcoma Omim
      A number sign (#) is used with this entry because the Ewing sarcoma family of tumors (ESFT) involve translocations of the EWS gene (133450) on chromosome 22q12 with various members of the ETS (see 164720) family of transcription factors. Description The Ewing sarcoma family of tumors (primitive neuroectodermal tumors; PNET) comprise morphologically heterogeneous tumors that are characterized by nonrandom chromosomal translocations involving the EWS gene on chromosome 22q12 and one of several members of the ETS family of transcription factors. The tumors include Ewing sarcoma, peripheral neuroepithelioma, and Askin tumor. In approximately 90% of cases of ESFT, the FLI1 gene (193067) on chromosome 11 is the fusion partner of EWS; in approximately 10%, the EWS fusion partner is the ERG gene (165080) on chromosome 22. Many other ETS family members have been identified as fusion partners of EWS, but these cases are rare (Khoury, 2005).
    • Ewing Sarcoma Mayo_clinic
      Overview Ewing (YOO-ing) sarcoma is a rare type of cancer that occurs in bones or in the soft tissue around the bones. Ewing sarcoma most often begins in the leg bones and in the pelvis, but it can occur in any bone. Less often, it starts in the soft tissues of the chest, abdomen, limbs or other locations. Ewing sarcoma is more common in children and teenagers, but it can occur at any age. Major advancements in the treatment of Ewing sarcoma have helped to improve the outlook for people with this cancer.
    • Ewing Sarcoma Gard
      Ewing sarcoma is a type of cancerous tumor that mainly affects children and young adults. Ewing sarcoma usually occurs in the long bones of the arms and legs, pelvis, or chest. Symptoms may include swelling over the location of the tumor, and pain which gets worse over time. Other symptoms may depend on the size and location of the tumor. Ewing sarcoma can spread to other parts of the body ( metastasize ), and other symptoms may develop such as fever, night sweats, and tiredness. The cause of Ewing sarcoma is unknown. Diagnosis is based on a clinical examination, health history, imaging studies, and blood tests.
    • Skeletal Ewing Sarcoma Orphanet
      Ewing's sarcoma is a malignant small round cell bone tumor with strong metastatic potential. Epidemiology Annual incidence is estimated at 1/312,500 in children under the age of 15. Clinical description It occurs between the ages of 5 and 30 with a peak of incidence between ages 12 and 18. The most frequent symptom is pain. Other symptoms depend on the organs closest to the tumor: motor, sphincteric disorders caused by nervous compression or mechanical disorders are associated with pelvic tumors; respiratory disorders or pleural effusion are associated with costal tumors; medullar or radicular compression are associated with vertebral tumors. The tumor initially develops most frequently in bone, particularly in the pelvis (30%), thorax (rib, clavicle, scapula) (20%), femur (16%), tibia (9%), vertebrae (8%) and humerus (5%).
  • Abortion In Colombia Wikipedia
    The court said it did not have enough arguments to issue the Judgment. [8] References [ edit ] ^ a b c d e f g h i j k l m n o p q r s t u v w x Sentencia C-355/06 (Constitutional Court 10 May 2006). ^ a b c Molina Betancur, Carlos Mario (2006).
  • Opioid Use Disorder Wikipedia
    Retrieved 16 July 2018 . ^ a b c d e f g h i j k l m n o p q r s t u v w x y z American Psychiatric Association (2013), Diagnostic and Statistical Manual of Mental Disorders (5th ed.) , Arlington: American Psychiatric Publishing, pp. 540–546 , ISBN 978-0890425558 ^ a b c d e f g h Substance Use and Mental Health Services Administration (30 September 2014). ... Retrieved 16 July 2018 . ^ a b c d e f g h i j k l Sordo L, Barrio G, Bravo MJ, Indave BI, Degenhardt L, Wiessing L, Ferri M, Pastor-Barriuso R (April 2017). ... ISBN 9780890425541 . ^ a b Shah, Mansi; Huecker, Martin R. (2019), "Opioid Withdrawal" , StatPearls , StatPearls Publishing, PMID 30252268 , retrieved 21 October 2019 ^ a b c d e f g h i j k Ries RK, Miller SC, Fiellin DA (2009). ... PMID 25083822 . S2CID 19157711 . ^ Blum K, Werner T, Carnes S, Carnes P, Bowirrat A, Giordano J, Oscar-Berman M, Gold M (2012). ... ADDICT DISORD THEIR TREAT. 2019;18(4):246-248. doi:10.1097/ADT.0000000000000175. ^ Bruneau J, Ahamad K, Goyer MÈ, Poulin G, Selby P, Fischer B, Wild TC, Wood E (March 2018).
    C9, CES1, PENK, TTC9, NAV3, BMPER, RGS2, RGS4, RGS10, DRD1, GHSR, HCRT, IL4, OPRM1, TLR4, PART1
  • Dentin Hypersensitivity Wikipedia
    Retrieved 21 December 2013 . ^ a b c d e f g h i j k l m n o Miglani, Sanjay; Aggarwal, Vivek; Ahuja, Bhoomika (2010).
    CPP, BAG1, RTN3, SMIM10L2A, CPAT1, ISYNA1, CPNE7, SLC27A4, DHS, DMTF1, DMP1, SAFB, RARB, NDUFAB1, MSN, GFAP, F8, EMP1, SMIM10L2B
  • Disorders Of Sex Development Wikipedia
    . ^ Jordan-Young RM , Sönksen PH, Karkazis K (April 2014). "Sex, health, and athletes" . ... ISBN 978-0-306-46759-2 . [ page needed ] ^ Röttger, S., K. Schiebel, G. Singer, S. Ebner, W. Schempp, and G. Scherer. Röttger, S., K. Schiebel, G. Singer, S. Ebner, W.
    HSD17B3, LHCGR, PPP1R12A, AKR1C3, AKR1C1, AKR1C2, DHCR7, NR5A1, SRY, SOX9, AR, STAR, RSPO1, TSPY1, SRD5A2, SOX10, AMH, CYP2B6, GATA4, MAP3K4, TSPY3, CBX2, HHAT, WWOX, QPCT, GADD45G, MAMLD1, PPIG, CYP11A1, WNT5A, TSPYL1, CYP17A1, CYP19A1, DECR1, DMRT1, FGF9, FOXF2, KLK3, TSPY10
  • Adult Attention Deficit Hyperactivity Disorder Wikipedia
    . ^ a b Antshel KM, Hargrave TM, Simonescu M, Kaul P, Hendricks K, Faraone SV (June 2011). "Advances in understanding and treating ADHD" . ... PMID 22976615 . ^ Fayyad J, De Graaf R, Kessler R, Alonso J, Angermeyer M, Demyttenaere K, et al. (May 2007). "Cross-national prevalence and correlates of adult attention-deficit hyperactivity disorder" .
    BDNF, CDH13, TPH2, SCLY, ADGRL3, CLOCK, ADIPOQ, LIN7A, SYN3, TAL1, SNAP25, SLC6A4, SLC6A3, SLC6A2, KRT7, HTR1A, DRD5, DRD4, DRD3, DGKH
  • Gender Dysphoria In Children Wikipedia
    ISBN 978-0323221528 . ^ a b Marcdante K, Kliegman RM (2014). Nelson Essentials of Pediatrics E-Book . ... Retrieved August 28, 2018 . ^ Alderson K (2012). Counseling LGBTI Clients . ... Journal of Sex and Marital Therapy , Volume 31, Number 1, January–February 2005, pp. 31-42(12) ^ Wilson K (1998). The Disparate Classification of Gender and Sexual Orientation in American Psychiatry 1998 annual meeting of the American Psychiatric Association, Workshop IW57, Transgender Issues, Toronto Canada, June. ^ Wilson, I; Griffith, C; Wren, B (2002). ... Retrieved 2008-06-14 . ^ a b c d Bryant, K (2006). "Making gender identity disorder of childhood: Historical lessons for contemporary debates". Sexuality Research & Social Policy . 3 (3): 23–39. doi : 10.1525/srsp.2006.3.3.23 . S2CID 144613679 . ^ Winters, K. (2008). "Gender Madness in American Psychiatry: Essays from the struggle for dignity".
  • Mandibular Fracture Wikipedia
    Open reduction was described as early as 1869. [40] Since the late 19th century, modern techniques including MMF (see above) have been described with titanium based rigid internal fixation becoming commonplace since the 1970s and biodegradable plates and screws being available since the 1980s. [ citation needed ] References [ edit ] ^ a b c d e f g h i j k l m n o p q r Murray, JM (May 2013). ... ISBN 978-0-323-02001-5 . ^ Nair, M. K.; Nair, U. P. (2001). "Imaging of mandibular trauma: ROC analysis" . ... PMID 15915103 . S2CID 11089616 . ^ Abdel-Galil, K.; Loukota, R. (2010). "Fractures of the mandibular condyle: Evidence base and current concepts of management". ... PMID 7999738 . ^ Kyrgidis, A.; Koloutsos, G.; Kommata, A.; Lazarides, N.; Antoniades, K. (2013). "Incidence, aetiology, treatment outcome and complications of maxillofacial fractures.
  • Psychopathy Wikipedia
    Mental disorder characterized by persistent antisocial behavior, impaired empathy and remorse, and bold, disinhibited, and egotistical traits Psychopathy Pronunciation / s aɪ ˈ k ɒ p ə θ i / Specialty Psychiatry , clinical psychology Symptoms Boldness , lack of empathy , inclination to violence and manipulation , impulsivity Causes Genetic and environmental Risk factors Family history , poverty , being neglected by parents Differential diagnosis Sociopathy , Narcissism , Machiavellianism , Sadism , Borderline personality disorder , Bipolar disorder (mania) Prognosis Poor Frequency 1% of general population Personality disorders Cluster A (odd) Paranoid Schizoid Schizotypal Cluster B (dramatic) Antisocial Borderline Histrionic Narcissistic Cluster C (anxious) Avoidant Dependent Obsessive–compulsive Not specified Depressive Haltlose Immature Passive–aggressive Cyclothymic Psychopathy v t e Psychopathy , sometimes considered synonymous with sociopathy , is traditionally a personality disorder characterized by persistent antisocial behavior , impaired empathy and remorse , and bold , disinhibited , and egotistical traits . [1] [2] [3] Different conceptions of psychopathy have been used throughout history that are only partly overlapping and may sometimes be contradictory. [4] Hervey M.
    MAOA, FLT4, PKD2L1, SLC6A4, DRD2, ANKK1, ALLC, CCHCR1, EIF2AK1, CCRL2, ALDH2, MAOB, MTA2, OXTR, HTR2A, STIN2-VNTR, BDNF, EXT1, TNF, CYP2E1, CRP, HGS, HTR3B, CAT, ADAMTS2, BAG3, SIRT1, AVPR1A, TGFB1, CCAR1, AVP, LRFN2, COL25A1, EBPL, SLC22A12, OR2AG1, ANK3, LINC00951, THAS, SNAP25, FAAH, HTR2B, FGD1, FKBP5, ELK3, GABBR1, GABRA2, GAD1, HARS1, HTR1B, ATN1, IARS1, DBH, IL10, DRD5, DRD4, NTRK2, ACE, POMC, PRL, ROBO2, SRSF5, ADH1B
    • Antisocial Personality Disorder Mayo_clinic
      Overview Antisocial personality disorder, sometimes called sociopathy, is a mental health condition in which a person consistently shows no regard for right and wrong and ignores the rights and feelings of others. People with antisocial personality disorder tend to purposely make others angry or upset and manipulate or treat others harshly or with cruel indifference. They lack remorse or do not regret their behavior. People with antisocial personality disorder often violate the law, becoming criminals. They may lie, behave violently or impulsively, and have problems with drug and alcohol use. They have difficulty consistently meeting responsibilities related to family, work or school.
    • Antisocial Personality Disorder Wikipedia
      S2CID 40789985 . ^ Loeber R, Keenan K, Lahey BB, Green SM, Thomas C (August 1993).
  • Prelabor Rupture Of Membranes Wikipedia
    ISBN 9780195189384 . ^ a b c d e f g h i j k l m n o p q r s t u v Committee on Practice, Bulletins-Obstetrics. ... The Global Library of Women's Medicine . doi : 10.3843/GLOWM.10120 . ^ a b c d e f g h i j k l m n o p q r Beckmann, Charles (2010). ... ISBN 978-0781788076 . ^ a b c d e f g h i j k l m n o p q r s t u v DeCherney, Alan (2013). ... ISBN 978-0071638562 . ^ a b c d e f g h i j k l m n o p q Cunningham, F (2014). ... ISBN 978-0071798938 . ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah "Practice Bulletins No. 139".
    SERPINH1, LMNA, OTX2-AS1, LINC01239, LINC02153, STK35, C10orf90, SHISAL1, TMEM241, SPATA6, ATP6V0A2, ZMPSTE24, VGLL4, ADAMTS2, SLIT2, RNASET2, TBCD, PLOD1, LPP, SLC7A14-AS1, RELA, NFKB1
  • Polysubstance Dependence Wikipedia
    ISBN 978-0-495-09557-6 . ^ a b c d e Medina, K; Shear, PK; Schafer, J; Armstrong, TG; Dyer, P (2004). ... Archived from the original on November 13, 2011. ^ Agrawal, Arpana; Lynskey, Michael T.; Madden, Pamela A. F.; Bucholz, Kathleen K.; Heath, Andrew C. (2007). "A latent class analysis of illicit drug abuse/dependence: Results from the National Epidemiological Survey on Alcohol and Related Conditions".
    CNR1
  • Osteonecrosis Of The Jaw Wikipedia
    PMID 15485717 . ^ Yajima D; Motani H; Kamei K; Sato Y; Hayakawa M; Iwase H (2006).
    APEX1, ACE, HAP1
    • Osteonecrosis Of The Jaw Orphanet
      A rare osteonecrosis characterized by an exposed necrotic lesion in the mandible or maxilla present for more than eight weeks, arising as a complication of antiresorptive medication, dental interventions, or trauma and infections. Patients may present with pain, altered neurosensory functions, secondary infections, and (in advanced stages) pathological fractures, or fistulae.
  • Sadomasochism Wikipedia
    Find sources: "Sadomasochism" – news · newspapers · books · scholar · JSTOR ( August 2014 ) ( Learn how and when to remove this template message ) ( Learn how and when to remove this template message ) Joe Shuster (1950s), co-creator of Superman , from Nights of Horror A male dominant whipping a female submissive while another woman watches ( Paris , 1930) Sadomasochism ( / ˌ s eɪ d oʊ ˈ m æ s ə k ɪ z əm / SAY -doh- MASS -ə-kiz-əm ) [1] is the giving and receiving of pleasure from acts involving the receipt or infliction of pain or humiliation . [2] Practitioners of sadomasochism may seek sexual gratification from their acts.
  • Grapefruit–drug Interactions Wikipedia
    Retrieved 21 November 2006 . ^ "Synonymy of C. reticulata at The Plant List" . ^ Larry K. Jackson and Stephen H. Futch (10 July 2018). ... ISSN 0269-4727 . PMID 10583697 . ^ Sugimoto K, Araki N, Ohmori M, et al. (March 2006). ... PMID 9264312 . ^ Preissner S, Kroll K, Dunkel M, et al. (January 2010). ... PMID 25547640 . ^ Samojlik, I.; Rasković, A.; Daković-Svajcer, K.; Mikov, M.; Jakovljević, V. (1 July 1999). ... PMID 22286159 . ^ Lilja JJ, Laitinen K, Neuvonen PJ (September 2005). "Effects of grapefruit juice on the absorption of levothyroxine" .
  • Cryptorchidism Wikipedia
    Recent Advances in Small Animal Reproduction . Retrieved 2006-08-10 . ^ Scott K, Levy J, Crawford P (2002). "Characteristics of free-roaming cats evaluated in a trap-neuter-return program".
    INSL3, RXFP2, CASP3, ATRX, CBL, CHRM3, HSD3B2, STS, PUM1, BCL2L1, GPX4, ESR1, HSF1, GFER, KDM5A, SYNE2, MSX1, HTRA2, ANXA5, FAS, AR, IGF1R, AMH, NR5A1, FGFR1, DAZ1, SRY, CYP19A1, RAF1, PTPN11, AMHR2, HOXD13, WT1, FGF8, OPHN1, TACR3, TAC3, ARNT2, PROKR2, OCRL, STAR, CHD7, CYP17A1, CYP11A1, GNRHR, SOS1, KISS1R, EBP, GATA4, RBMY1A1, FLNA, ANOS1, MECP2, EED, ACTB, NR0B1, PWAR1, SEC24C, OGT, ORC6, PEX3, NPAP1, FLRT3, RAB3GAP2, NIPBL, LMOD1, ATP6V0A2, RTTN, SIN3A, C2CD3, NSMF, CNTNAP2, PIGN, NNT, IFT172, TP63, SZT2, PTCH2, SYNE1, SMCHD1, SPECC1L, MED13L, ADNP, KAT6B, ZFPM2, KCNAB2, GRIP1, GPR161, TGDS, SUZ12, AUTS2, CUL4B, PHGDH, WDPCP, POMT2, SLC25A24, DHH, CDON, TBX22, GMNN, POLR1D, RPGRIP1L, KDM5C, KMT5B, RLIM, CCDC174, TMEM216, DACT1, GMPPB, ANKRD11, UBE2T, SETD2, CCDC22, BBS9, AFF4, ACTA1, B9D1, TBL2, TINF2, NAA10, HIBCH, USP9Y, ARID1A, TRRAP, CDC45, NEDD4L, DDX3Y, SEMA3E, APC2, HUWE1, GPC6, MKRN3-AS1, CD96, IRX5, STAG1, RXYLT1, LARGE1, SMC3, BAZ1B, CITED2, SEMA3A, EMG1, MAD2L2, HACD1, MAMLD1, PACS2, PEX16, GTF2IRD1, TMEM94, PTDSS1, LRIG2, FIG4, POLR1C, MED12, TRIP4, RECQL4, HS6ST1, SRA1, COG1, NRXN1, LONP1, COG5, SEC23A, POMT1, TRIM32, B4GALT7, MRAS, CILK1, RAB3GAP1, SGPL1, RAB18, PHF8, TXNRD2, KDM6B, ANKLE2, FGF17, SLC35D1, HESX1, PEX11B, POLR3A, AP1S2, BCL10, B4GAT1, IFT27, KCNQ1OT1, MAPRE2, HERC2, CLP1, PNPLA6, MBTPS2, SDCCAG8, GJB6, KDM5B, DLL3, BRSK2, CTCF, CPLX1, ABL1, DYNC2LI1, OTUD6B, TMEM67, ATPAF2, ALKBH8, BBIP1, G6PC3, CHST14, TOE1, TTC8, TBC1D20, DIS3L2, BBS5, DNAJC19, EVC2, DNAJC21, RIPPLY2, MPLKIP, NKX2-6, WDR34, LHX4, POMGNT2, PLVAP, FUZ, KLHL15, B9D2, CDT1, VANGL1, SPRY4, LAS1L, CDCA7, HES7, BRIP1, ARL6, POMK, PHF6, UQCC2, TMEM107, SLX4, GATA5, A2ML1, B3GLCT, FREM2, NALCN, H19, KANSL1, CCDC141, DOK7, SNORD115-1, RSPO2, KIF7, EBF3, FEZF1, MYMK, GTF2H5, CRPPA, PWRN1, SNORD116-1, RNU4ATAC, BRWD3, STAC3, GSC, VPS13B, MESP2, CCBE1, B3GALNT2, CKAP2L, CEP120, ESCO2, C8orf37, BBS12, PHACTR1, ARX, ARID2, UBR1, STT3B, TUBB, HYLS1, JMJD1C, CEP290, FRAS1, DHDDS, PACS1, CEP55, SETD5, ATAD3A, BBS7, FANCI, POMGNT1, PEX26, VAC14, FANCL, POLR3B, WDR11, MBD5, MCTP2, HDAC8, ASH1L, KMT2E, RFWD3, WDR60, DAZ3, MAGEL2, SUFU, RAB23, WWOX, MAP3K20, FGFRL1, RIN2, TMCO1, LZTFL1, PHIP, IL17RD, SAMD9, BCOR, NSUN2, MKS1, TMEM70, LZTR1, MRAP, DAZ2, TCTN2, THOC6, MTMR14, PORCN, COLEC11, ALG8, FTO, ALG12, FKRP, TMEM231, LMBR1, FAT4, DYNC2H1, TBL1XR1, PALB2, BBS10, EHMT1, CSPP1, NXN, NSD1, HYMAI, ZSWIM6, RPGRIP1, DAZ4, SELENON, ARID1B, WDR35, CC2D2A, IFT80, FANCM, STRA6, DMRT3, HPSE2, ALX4, PROK2, PIEZO2, PRDM16, SMOC1, RBM10, SMC1A, MKKS, GLI1, GATA6, GDF1, GJA5, GJB2, GPC3, GLE1, GLI2, GABRD, GLI3, GNRH1, GP1BB, GRIA3, GTF2E2, GTF2I, GATA1, FZD2, FANCC, GPC4, FANCE, FANCB, FANCF, FANCG, FBN1, FKTN, FGD1, MTOR, FGF14, FGFR3, FGFR2, FLI1, FLNB, FMR1, HBA1, HBA2, HNRNPK, KMT2A, LIMK1, SMAD4, MC2R, MEFV, MAP3K1, MID1, MTM1, HRAS, MUSK, MYF6, MYH3, MYH11, MYL2, MYLK, LIG4, LHX1, LFNG, LETM1, KRAS, KIT, KISS1, KCNQ1, STT3A, ITGA7, IRF6, IPW, INSR, INPPL1, IGF2, HSPG2, HSD17B3, FANCD2, FANCA, NDN, CDH11, BRCA2, BUB1B, MYRF, TMEM258, CDC6, CDC42, CDKN1C, BRCA1, CHD4, AKR1C4, CHRNG, ERCC8, CLCN4, COL3A1, BRAF, BMP4, EZH2, ARVCF, ACTA2, ACTG2, AEBP1, JAG1, BIN1, ANK1, RERE, BLM, ATR, AXL, BBS1, BBS2, BBS4, BDNF, COL4A1, COL6A1, COMT, EP300, DVL1, DVL3, EFNB1, MEGF8, EIF2S3, ELN, ERCC2, CREBBP, ERCC3, ERCC4, ERCC5, ERCC6, EVC, EXT2, DUSP6, SLC26A2, ATN1, DNMT3A, DNM2, DMPK, DLX4, DKC1, DHODH, DHCR7, AKR1C2, DDB2, DCC, DAG1, CYB5A, CTBP1, NKX2-5, MYOD1, H19-ICR, NDP, SMARCB1, XRCC2, ROBO1, RPL10, XPC, RRAS, RREB1, XPA, WNT7A, RYR1, WNT5A, SALL1, SKI, NF1, WNT3, SMARCA2, RIT1, RFC2, DPF2, RAD51C, PEX5, PYCR1, RAC1, RAD21, RAD51, ZBTB16, MKRN3, RASA2, YY1, RAP1A, RAP1B, XRCC4, RAPSN, RARB, SMARCA4, SMARCC2, PEX19, SMARCE1, HNF1B, TCOF1, TFAP2A, NSD2, TPM2, TPM3, WHCR, TSPY1, TSPYL1, HIRA, TWIST1, UBA1, UBE2A, CLIP2, KDM6A, TBX3, TCF4, TBCE, SOX9, SMS, SNRPN, SOS2, SOX2, SOX3, SOX4, NELFA, TBX1, SOX10, SOX11, SRD5A2, STK11, VAMP7, TAF6, PEX2, UFD1, PEX1, NRAS, PMM2, RNF113A, PIK3CA, PIK3C2A, PEX14, PEX13, NUP88, SIX6, ORC1, ORC4, OTX2, PEX12, PAX6, PEX10, PEX6, PTCH1, PBX1, PDE4D, KAT6A, ROR2, PLAGL1, TUBA1A, MAP2K2, MAP2K1, PRKAR1A, POLD1, PPP1CB, SHOC2, NPHP1, NOTCH3, POR, POLE, NOTCH2, KMT2D, SSTR4, LPAR2, ACKR3, GPR42, EDNRA, CXCR6, BRS3, ADRA1A, ADRA2B, HOXA10, TGCT1, MMP11, POU5F1P3, EGR4, POU5F1P4, GPRC6A, SLC22A3, BRD2, SOD1, AZF1, GGCT, HOXA11, POU5F1, ZNF214, ZNF215, AHR, FZD4, MKX, KIR2DS2, CD44, FCGR1CP, MRGPRX1, USP1, IL27, UTF1, CFTR, ATP2B1, ATP2A1, CAT, CALCA, IL31, AXIN1, GPR166P, VN1R17P, NANOS2, OXER1, NR1I2, STRA8, MIR34C, RBMY2DP, ALPG, MIR210, RBMY1D, BAX, SPAG5, PIWIL4, PDE4A, STRBP, IGFBP3, PGK2, LPAR3, MARCHF1, HMGA2, KIR2DS1, KIR3DL2, LCN2, PDE4B, LHCGR, DUOX1, IL17D, HLA-DRB1, LIFR, REG3A, MMP1, MMP2, NUMA1, MYH2, DKKL1, MYH7, IL22, SYCP3, NOX4, DUOX2, HSPA4, HLA-DQB1, UCHL1, SLC52A2, CIRBP, GPR151, TPT1, GTSF1, MRGPRX4, MRGPRX3, TGFBR3, ST13, E2F1, F2R, PAICS, PLK4, FCGR1A, MYDGF, FCGR1B, RPL29, HHIP, GART, LGR6, IL21, PTBP2, MIER1, GHSR, PTGDS, NPBWR2, PRDM9, PARPBP
    • Cryptorchidism, Unilateral Or Bilateral Omim
      A number sign (#) is used with this entry because of evidence that cryptorchidism can be caused by heterozygous mutation in the insulin-like-3 gene (INSL3; 146738) on chromosome 19p13. Description Cryptorchidism, or failure of testicular descent, is a common human congenital abnormality with a multifactorial etiology that likely reflects the involvement of endocrine, environmental, and hereditary factors. Cryptorchidism can result in infertility and increases risk for testicular tumors. Testicular descent from abdomen to scrotum occurs in 2 distinct phases: the transabdominal phase and the inguinoscrotal phase (summary by Gorlov et al., 2002). Clinical Features Bishop et al. (1979) pointed out that renal anomalies such as renal agenesis are often associated with the familial form of cryptorchidism.
    • Undescended Testicle Mayo_clinic
      Overview A testicle that doesn't move down into its proper place in the scrotum before birth is called an undescended testicle. It's also known as cryptorchidism (krip-TOR-kih-diz-um). Most often, it's just one testicle that doesn't descend into the scrotum, which is the bag of skin that hangs below the penis. But sometimes both testicles are affected. An undescended testicle is more common in premature babies than it is in full-term infants. An undescended testicle often moves down on its own within a few months after the baby is born. If your baby has an undescended testicle that doesn't correct itself, surgery can be done to move the testicle into the scrotum.
  • Apathy Wikipedia
    .; Lockwood, P.; Apps, M.A.; Muhammed, K.; Husain, M. (2017). "Distinct Subtypes of Apathy Revealed by the Apathy Motivation Index" .
    GRN, TBK1, MAPT, ACAT1, DNAJC6, TARDBP, ATP13A2, DNAJC13, PARK7, SQSTM1, CHMP2B, VCP, UCHL1, SPAST, SNCA, PSEN1, ATXN10, GIGYF2, PRKAR1B, COQ2, HTRA2, TREM2, TMEM106B, VPS13C, VPS35, JPH3, PINK1, EHMT1, LRRK2, HGSNAT, C9orf72, TMEM240, CHCHD10, PRNP, SMARCB1, PODXL, CACNA1A, FUS, DNMT1, GBA, PDGFB, DCTN1, GM2A, HEXA, CSF1R, HLA-DQB1, HMGCL, EIF4G1, PRKN, APOE, MCIDAS, ACHE, CSF2, SLC6A4, LAMC2, TLE5, SLC6A3, COMT, DRD1, USH1G, AR, BDNF, PRX, DRD3, CRP, PRND, DRD4, CFLAR, SGCA, MSN, SOD1, MC4R, LIPA, TRPV1, IGFALS, ENPEP, ADAMTS2, RAPGEF4, MAPK8IP3, HCRT, SMUG1, TPSG1, NPS
  • Mullerian Anomalies Wikipedia
    PMID 22049383 . ^ Chan YY, Jayaprakasan K, Zamora J, Thornton JG, Raine-Fenning N, Coomarasamy A (2011). ... PMID 18539641 . ^ a b c d e f Cheroki C, Krepischi-Santos AC, Szuhai K, Brenner V, Kim CA, Otto PA, Rosenberg C (April 2008). ... PMID 24050215 . ^ a b Heinonen PK, Kuismanen K, Ashorn R (April 2000). "Assisted reproduction in women with uterine anomalies". ... PMID 11699126 . ^ Chan YY, Jayaprakasan K, Tan A, Thornton JG, Coomarasamy A, Raine-Fenning NJ (October 2011).
  • Subcutaneous Emphysema Wikipedia
    PMID 6375617 . ^ a b c d e f g h i j k l m n o Parker GS, Mosborg DA, Foley RW, Stiernberg CM (September 1990).
  • Externalizing Disorders Wikipedia
    PMID 16351376 . ^ a b c d e f g h i j k l m n o p q r s t u "Disruptive, Impulse-Control, and Conduct Disorders".
  • Echinococcosis Wikipedia
    PMID 12643838 . ^ a b c d e John, David T.; William Petri, William A.; Markell, Edward K.; Voge, Marietta (January 2006). "7: The Cestodes: Echinococcus granulosus , E. multiloularis and E. vogeli (Hyatid Disease)" . ... Lancet Infect Dis . 7 (6): 385–94. doi : 10.1016/S1473-3099(07)70134-2 . PMID 17521591 . ^ Dang Z, Yagi K, Oku Y, et al. (December 2009). "Evaluation of Echinococcus multilocularis tetraspanins as vaccine candidates against primary alveolar echinococcosis". ... PMC 2768250 . PMID 19881979 . ^ Jani K (July 2014). "Spillage-free laparoscopic management of hepatic hydatid disease using the hydatid trocar canula" . ... Archived from the original on 24 September 2015. ^ Lassen, B.; Janson, M.; Viltrop, A.; Neare, K.; Hütt, P.; Golovljova, I.; Tummeleht, L.; Jokelainen, P. (2016). ... PMID 27723790 . ^ Marcinkutė, A.; Moks, E.; Saarma, U.; Jokelainen, P.; Bagrade, G.; Laivacuma, S.; Strupas, K.; Sokolovas, V.; Deplazes, P. (2015).
    ALB, HBB, TF, TNF, MIR19B1, GSTK1, PRSS55, SLCO6A1, SPZ1, EPC1, CRISP2, THBS1, TLR4, CYP1A1, CYTB, COX1, IL17A, IL9, HLA-G, EDNRB, RN7SL263P
    • Cystic Echinococcosis Orphanet
      Hydatidosis or cyst hydatic disease is a cosmopolitan larval cestodosis caused principally by the Echinococcus granulosus tapeworm, the adult form of which parasitises the intestine of dogs. Hydatidosis generally affects large domestic herbivores; humans are dead-end hosts, infected through contact with herding dogs or through ingestion of food contaminated with canine excrement. Epidemiology The annual incidence of human infection in Europe is around 1/100 000 but the disease is more common other countries such as Uganda, Sudan and Ethiopia where the prevalence is estimated at between 1 and 3.2% of the general population. Clinical description After ingestion, the larvae develop very slowly, forming cysts that are not diagnosed until 10 to 20 years after contamination. The liver (60% of cases), lungs (30% of cases) and other organs (kidneys, spleen, brain etc ) are the principle sites of cyst formation.
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