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Postural Orthostatic Tachycardia Syndrome
Wikipedia
Propranolol (Inderal) [94] [95] [96] beta-blockers (Selective) Metoprolol (Toprol), [87] [97] Bisoprolol [98] [92] Selective sinus node blockade Directly reducing tachycardia. Ivabradine [83] [84] [99] [100] alpha-2 adrenergic receptor agonist Decreases blood pressure and sympathetic nerve traffic. ... S2CID 11628648 . ^ 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 Mathias CJ, Low DA, Iodice V, Owens AP, Kirbis M, Grahame R (December 2011). ... Indian Pacing and Electrophysiology Journal . 6 (2): 84–99. PMC 1501099 . PMID 16943900 . ^ Mallien J, Isenmann S, Mrazek A, Haensch CA (2014-07-07). ... Indian Pacing and Electrophysiology Journal . 6 (2): 84–99. PMC 1501099 . PMID 16943900 . ^ Kavi L, Gammage MD, Grubb BP, Karabin BL (June 2012).
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Intraductal Papillary Mucinous Neoplasm
Wikipedia
Diagnosis [ edit ] Histopathology of IPMN types in a distal pancreatectomy specimen from a 60-year-old man, by gross pathology (center image), microscopy and immunohistochemistry : The resected specimen (c) revealed that the mural nodule in the MPD consisted of PB-type IPMN with high-grade dysplasia (adenocarcinoma) (a) with a diffuse positivity of p53 immunostaining (an insert) and KRAS mutation (G12V). The BD-IPMN of the body was lined by gastric mucinous epithelium showing low papillary configuration with mild epithelial stratification with the same KRAS mutation (d), and the proliferation of similar gastric IPMN components sequentially involved the bottom of the mural nodule and the wall of the surrounding dilated MPD (indicated by red arrowheads) (b). The BD-IPMN of the tail was lined by flat, monolayer gastric mucinous epithelium lacking cellular atypia and KRAS mutation (e). [4] In most cases, IPMNs are diagnosed based on clinical and radiographic criteria. [5] If fluid from the cyst is aspirated, the CEA level is typically elevated. [5] Confirmation of the diagnosis with tissue is rarely necessary. [5] By histopathology , IPMN is characterized on light microscopy by Mucinous epithelial cells, [6] and growth within the pancreatic ducts . [7] Mucin 5AC is a useful immunohistochemistry marker. [8] Characteristic genetic alterations are those of KRAS and GNAS . [8] Further subtyping of IPMN can be done as either: [9] Gross pathology : Main duct, branch duct, and mixed duct lesions, which determines surgical management. ... A study using Surveillance, Epidemiology, and End Results Registry (SEER) data suggested that increased lymph node counts harvested during the surgery were associated with better survival in invasive IPMN patients. [15] Prognosis [ edit ] Survival 5 years after resection of an IPMN without malignancy is approximately 80%, 85% with malignancy but no lymph node spread and 0% with malignancy spreading to lymph nodes. [16] Epidemiology [ edit ] Side branch IPMNs are the most common pancreatic cysts. [5] IPMNs occur more often in men than women, and often occur in the 6th and 7th decade of life.GNAS, KRAS, MUC1, BRAF, ERBB2, SMARCA4, PIK3CA, ANXA10, LMO4, AIP, LONP1, GDF15, MSLN, POSTN, HHLA2, AQP4, SMUG1, VEGFA, SETD2, RMC1, NSD1, PPP1R2C, SNORD35B, SNORD14B, SNORD14C, SNORD14D, SNORD14E, MIA, ZEB1, TP53, MSH2, CFTR, CTNNB1, EGFR, FGF6, MSH6, IL1B, LEP, SMAD4, MUC2, TNF, MUC5AC, NPTX2, PIM1, PTEN, SNORD15A, SKIL, SPINK1, THBS2, MIR1290
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Taurodontism
Wikipedia
Here a tooth is tarodont if AB/AC >= 0.2 and BD > 2.5mm (A: Lowest point of the roof of the pulp chamber. ... Pp. 147-148,473-478.L ^ Shaw JC (1928) Taurodont teeth in South African races. Journal of Anatomy 62, 476–98. ^ Schiffman A, Chanannel I. Prevalence of taurodontism found in radiographic dental examination of 1200 young adult Israeli patients.
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Facial Femoral Syndrome
Wikipedia
J Clin Ultrasound 42(1):49-52 ^ Daentl DL, Smith DW, Scott CI, Hall BD, Gooding CA (1975) Femoral hypoplasia--unusual facies syndrome.
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Squamous-Cell Carcinoma Of The Lung
Wikipedia
Epidemiology [ edit ] Lung squamous-cell carcinoma is the second most common histologic type of lung cancer after adenocarcinoma, reaching 22.6% of all lung cancer cases as of 2012. [11] The relative incidence of the former has been steadily decreasing in favor of the latter due to the decreasing smoking rates in the last few years. [9] As much as 91% of lung SCC has been found to be attributable to cigarette smoking. ... "Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines" . Cell Systems . 6 (3): 271–281.e7. doi : 10.1016/j.cels.2018.03.002 .FGFR2, EGFR, DDR2, KRAS, EPHA2, FGFR1, IGF1R, TTN, PLK1, NOTCH1, FYN, PRKDC, DDR1, MAST4, EPHA3, MYLK4, EPHA5, ANKK1, WNK3, ACVR1C, GUCY2F, DCLK3, MAP3K15, AURKC, BMP2K, TRIM24, MYO18B, ERBB4, MAP2K4, MAP4K3, CSF1R, ATR, TP53, CDKN2A, PIK3CA, BRAF, FGFR3, NFE2L2, STK11, FBXW7, HLA-A, CHRNA3, CLPTM1L, HRAS, PTEN, EP300, HLA-DQA1, CYP2A6, HNF1B, DCLK1, KRT8, BRCA2, H2AC6, TNXB, HLA-B, DCUN1D4, PDS5B, THRB, ATXN2, TRIM26, DBH, HLA-DMB, GBAP1, FRY, RALY, ESM1, SH2B3, MORF4L1, HCP5, SOX2, ZSCAN12, SCGN, BTN3A3, ZNF623, GSTM1, PKD2L1, MED12, HLA-DQA2, NEB, LCORL, MORN5, GPX6, LINC-PINT, CENPP, PC, B2M, NF1, FAM155A, PPP6C, ALK, CDKN2B-AS1, ZSCAN16-AS1, MTX1, EGFR-AS1, MUC22, PTCSC2, TSBP1-AS1, CYP1A1, NEK10, BTBD9, VARS2, BABAM1, CD274, ZNRD1, RAD51B, LRRC8D, CARMIL1, CREBBP, PTPN11, REXO4, NPAS3, TUBA1C, WNK1, ZNF322, CHRNB4, USHBP1, PGBD1, KCNH1, APOM, PIK3CB, PIK3CD, PIK3CG, H3P10, TP63, NME1, GPC3, PTHLH, MIR205, MET, CEACAM5, VEGFA, RARB, GATA6, CCND1, MKS1, MAP2K7, MAPK3, BDNF, CDK4, SFTA1P, DSG3, MIR93, MYC, AKT1, CTNNB1, TYMS, RAD52, ME1, TOP2A, TGFBR2, ELAVL2, PDPN, OGG1, SOX2-OT, MALAT1, MIR145, MIR150, ZEB1, PDCD1, MIR21, MBD2, NAPSA, PARP1, PROM1, SUMO1P3, MIR375, MIR590, CXCR4, MPO, MMP9, MLH1, CCNB2, CKAP4, FGF19, RET, TPX2, TRIM58, DGCR5, HPGDS, SGSM3, RPE65, ROS1, RFC4, SLC2A2, UVRAG, SKP2, XAF1, PTPN13, ACKR3, PTK2, SST, DMRT3, PSG2, STAT3, PDCD1LG2, PRKCI, TIMP1, BMP4, CLDN3, COL11A2, ERBB2, CYP1A2, CYP2E1, FHIT, STMN1, IL6, FGFR4, LGALS8, CAV1, LOXL2, CDH1, EIF4G1, GABPA, BCL2, GSTP1, IFNG, DUSP6, CEACAM3, CEACAM7, MCL1, MDM2, SMAD4, AGER, CTLA4, GLI1, BIRC6, SOX17, AICDA, MYDGF, METTL3, COL17A1, SPC25, RAD18, SYT13, CLDN7, CCAR2, METTL14, COX8A, KIF15, MRTFA, CNOT6, NSD1, MEOX1, ZMAT3, DENND2D, ZNF503, CDKN1B, MAP1LC3A, HOPX, CHRNA4, FSD1L, DOCK8, MAP1LC3B, CHRNA7, CHUK, TBL1XR1, P2RY12, AP2M1, IRX1, FSD1, MAPKAP1, FTO, BRD9, CLU, CCR4, MRPL41, IL25, FRTS1, CRK, CPOX, LMO3, IL17C, LHX6, FBXO5, DAXX, PRPF31, POLDIP2, RNF19A, AKR1C2, NOCT, CIZ1, SNHG1, CORO1C, MMD, NCS1, SIRT1, COBL, GRAMD4, GADD45A, PEG10, DIO3, DMRT1, MMRN1, DNAH5, TUSC2, WIF1, IL17B, GPR78, RBMS3, CSNK2A1, BRK1, CACNA2D3, CHFR, HHAT, ATG4D, MAPK14, CSF1, BRF2, CSF2, CSF3, ALKBH5, EGLN1, TMEM97, CYTL1, SOX18, GPR87, IL17D, BCL11A, ANAPC11, GOLM1, GMNN, CSNK2A2, CTSB, EML4, RIOX2, IL17F, CDKN1A, MNX1-AS1, MIR193B, MIR452, MIR448, AQP5, ARG2, MIR372, MIR342, MIR324, MIR135B, MAP1LC3C, C5orf17, PRR26, MIR9-3, BCHE, MIR31, MIR29B2, MIR29B1, MIR29A, MIR28, MIR224, MIR223, MIR206, BMI1, MIR203A, MIR20A, MIR486-1, IGF2BP2-AS1, MIR195, LINC00273, SEC62-AS1, LINC01419, ADRA1A, ADRA2B, LINC01206, MIR5682, COMMD3-BMI1, LINC00968, AGTR1, PCAT6, MIR1911, ALB, GATA6-AS1, VPS9D1-AS1, MIR944, MIR541, ALDH1A1, MIR671, ANG, LINC00460, MIR662, ANGPT1, MIR588, MIR579, NME1-NME2, MIR198, MIR192, TRIM15, CD14, STXBP4, FAM83B, ADGRF4, CD44, FBXO45, PLPP4, FEZF1-AS1, APCDD1L-DT, IL23R, FAM163A, HJV, PIWIL4, LINC00261, ADHFE1, CD109, CDK2, PODN, LRRK2, CDK7, AZIN2, PRDM5, MUC16, MTDH, IL33, ERVH48-1, MS4A3, CCNE1, MIR185, TBX5-AS1, MIR183, MIR182, MIR15A, FOXL2, MIR144, MIR141, MIR140, MIR125A, MIRLET7I, BRS3, USP17L7, SERPING1, CCL4L1, KMT5A, CA9, CASP3, CASR, CBR1, GADL1, CELIAC2, STPG4, CXCL17, HCCAT5, SBF2-AS1, CCK, FSTL1, AHSA1, DSC3, S100A10, RRM2, RPS14, FOXA2, HNRNPU, RGS3, HOXA10, HSPB1, HTC2, IRF8, MOK, IFIT2, PVT1, PTPRA, IGF2R, TWF1, PTK7, IHH, PTGS2, IL10, IL17A, MASP1, IDO1, MAPK8, IRF1, MAPK1, S100A6, HLA-C, DUSP1, SERPINB3, GSTM2, STAT1, SSTR4, SRPK2, SRPK1, SQLE, SPARC, SOX4, GZMB, HLTF, HBE1, SLC2A1, HIC1, SIM1, SIAH2, SHH, SFTPB, TRA2B, SRSF2, SRSF1, HK2, SELENOP, SELP, CCL4, CCL2, IRF4, ITGB4, KIF5B, PPBP, NME2, NGFR, NFYC, NFKBIA, NFIX, LRP6, LRP5, EPCAM, NCAM1, MYO10, MYH10, MYCN, SMAD3, MYBPH, MUC4, MUC1, ND5, MSR1, MSH2, MMP14, MCM2, MMP7, MCM5, MIF, MIA2, LIPA, LGALS1, CLDN11, SERPINA1, POU4F2, POU3F2, KIT, PLG, PLAU, PKP1, PIK3R2, KRT19, KRT81, LCK, SERPINB5, ABCB1, OVOL1, PDGFRB, LCN2, PCNA, LDHA, PAX7, PARN, PAK1, SERPINE1, PAEP, PEBP1, P2RY1, AURKA, GSPT1, GSK3B, BECN1, CCL4L2, TP53I3, BAG4, EIF2AK3, GRAP2, COX5A, PLAA, KL, SOCS6, PIWIL1, ERCC1, LPAR2, ESRRA, CLDN1, CLDN12, PRC1, ETV4, H3C7, EZH2, SQSTM1, F2R, INPP4B, FAP, TNFRSF10B, DLK1, EPHX1, KMT2B, KEAP1, HCG9, E2F1, CHL1, CXCR6, ECT2, SPAG5, EDNRA, TACC3, YAP1, PIAS3, DLC1, EEF2, GPHN, EPHB3, WASF2, PDIA6, EIF4E, ARL4C, ARPC5, BCL2L11, HDAC5, ENO1, EPAS1, GAB2, ZEB2, TNFSF10, FGF1, MAP3K7, GAS7, FUS, FUT1, TTF1, NR2C2, TPD52, TOP3A, GATA3, GATA4, TNNI3, TNF, CLDN5, TK1, TIAL1, TIA1, GPR42, THOP1, THBS2, GPX2, TGFBI, TGFB1, TFF3, TFAM, TERC, GRN, GRM8, SUMO1, SCGB1A1, USP4, FGF9, FGF3, HYAL3, H3C2, H3C10, H3C12, H3C8, H3C11, H3C6, H3C3, H3C4, H3C1, FXR1, FOXO3, KMT2D, AIMP2, USP7, YWHAZ, XRCC3, XRCC1, XPC, WNT5A, VIM, FOXM1, VDAC3, ABL2
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Brachydactyly
Wikipedia
Contents 1 Types 2 Other syndromes 3 See also 4 References 5 External links Types [ edit ] There are several types of Brachydactyly: Type OMIM Gene Locus Also known as/Description Type A1, BDA1 112500 IHH BDA1B 5p13.3-p13.2, 2q33-q35 Brachydactyly type A1 or Farabee-type brachydactyly. ... The phalanges of the index fingers and second toes are shortened. Type A3, BDA3 112700 Brachydactyly type A3, Brachymesophalangy V or Brachydactyly-Clinodactyly. ... Type A6, BDA6 112910 Brachydactyly type A6 or Osebold-Remondini syndrome. Type A7, BDA7 Brachydactyly type A7 or Brachydactyly Smorgasbord type. [1] Type B, BDB (or BDB1) 113000 ROR2 9q22 Brachydactyly type B. ... Type A1B, BDA1B 607004 5p13.3-p13.2 Brachydactyly type A1, B. Other syndromes [ edit ] In the above brachydactyly syndromes, short digits are the most prominent of the anomalies, but in many other syndromes ( Down syndrome , Rubinstein-Taybi syndrome , etc.), brachydactyly is a minor feature compared to the other anomalies or problems comprising the syndrome. ... Cite journal requires |journal= ( help ) External links [ edit ] Classification D ICD - 10 : Q68.1 ICD - 9-CM : 755.2 - 755.4 MeSH : D059327 DiseasesDB : 29782 SNOMED CT : 43476002 Type A2 [ permanent dead link ] Brachydactyly type A1 at NIH 's Office of Rare Diseases Brachydactyly type A2 at NIH 's Office of Rare Diseases Brachydactyly type A3 at NIH 's Office of Rare Diseases Brachydactyly type A6 at NIH 's Office of Rare Diseases Brachydactyly type A7 at NIH 's Office of Rare Diseases Brachydactyly type B at NIH 's Office of Rare Diseases Brachydactyly type C at NIH 's Office of Rare Diseases Brachydactyly type E at NIH 's Office of Rare Diseases Brachydactyly types B and E combined at NIH 's Office of Rare Diseases v t e Congenital malformations and deformations of musculoskeletal system / musculoskeletal abnormality Appendicular limb / dysmelia Arms clavicle / shoulder Cleidocranial dysostosis Sprengel's deformity Wallis–Zieff–Goldblatt syndrome hand deformity Madelung's deformity Clinodactyly Oligodactyly Polydactyly Leg hip Hip dislocation / Hip dysplasia Upington disease Coxa valga Coxa vara knee Genu valgum Genu varum Genu recurvatum Discoid meniscus Congenital patellar dislocation Congenital knee dislocation foot deformity varus Club foot Pigeon toe valgus Flat feet Pes cavus Rocker bottom foot Hammer toe Either / both fingers and toes Polydactyly / Syndactyly Webbed toes Arachnodactyly Cenani–Lenz syndactylism Ectrodactyly Brachydactyly Stub thumb reduction deficits / limb Acheiropodia Ectromelia Phocomelia Amelia Hemimelia multiple joints Arthrogryposis Larsen syndrome RAPADILINO syndrome Axial Skull and face Craniosynostosis Scaphocephaly Oxycephaly Trigonocephaly Craniofacial dysostosis Crouzon syndrome Hypertelorism Hallermann–Streiff syndrome Treacher Collins syndrome other Macrocephaly Platybasia Craniodiaphyseal dysplasia Dolichocephaly Greig cephalopolysyndactyly syndrome Plagiocephaly Saddle nose Vertebral column Spinal curvature Scoliosis Klippel–Feil syndrome Spondylolisthesis Spina bifida occulta Sacralization Thoracic skeleton ribs : Cervical Bifid sternum : Pectus excavatum Pectus carinatumGNAS, HDAC4, SMAD4, TCTEX1D2, PTHLH, ROR2, HOXD13, FBN1, COL2A1, TRPS1, BMPR1B, GDF5, IHH, CHSY1, PDE3A, PRMT7, HOXA13, LMNA, PDE4D, NOG, PRKAR1A, PTCH1, PTH1R, TWIST1, FGFR3, ACAN, RUNX2, B3GLCT, GJB4, CCDC22, IFT172, TCTN3, SIN3A, POC1A, NIPBL, PIGN, KAT6B, ZFPM2, EXOSC2, ADNP, SIK3, SPECC1L, SLC35D1, AFF4, DCPS, TMEM216, KIF7, FAM149B1, IFT81, ANKRD11, SH3PXD2B, DONSON, EOGT, SCAPER, CHST11, KCNK4, TBX22, MRPS16, IFT52, ZDHHC9, PLXND1, POGZ, SPART, IFT140, WASHC5, KIAA0753, PTDSS1, KLLN, KIAA0586, RNU4ATAC, SEMA3E, IQSEC2, MACROH2A1, CHST3, EIF2AK3, ECEL1, CRIPT, LONP1, MAFB, MED12, HUWE1, BHLHA9, CWC27, MIR17HG, CITED2, SEC23B, DEAF1, STAMBP, RAI1, SRCAP, PNPLA6, POP1, MRAS, MYMK, CILK1, RLIM, ZDHHC24, TMEM256, NXN, EVC2, FTO, CPLANE1, UPF3B, PORCN, SIL1, PRDM16, CANT1, FAM111A, TRPV4, NLRC4, WDR19, DOCK6, IFT80, CCDC28B, DYNC2H1, TTC21B, EHMT1, BBS5, CSPP1, ADAMTS10, ARL6, COL25A1, WDR34, TMEM67, BBIP1, PIGS, IFT43, C12orf57, NLRP3, ANTXR2, WDR35, ARHGAP31, TBC1D24, CEP120, POMP, NBAS, DYNC2LI1, SUFU, ARID2, RAB23, INPP5K, WNT4, RIN2, ESCO2, MAGEL2, DLL4, LZTFL1, DYM, NSUN2, SNX14, IMPAD1, IFT57, WDR60, YY1AP1, SLC35C1, CHD7, IARS2, A2ML1, GATA5, IFT122, HDAC8, KIF15, NKX2-6, SLURP1, TRIP11, PTCH2, SMC3, GATA6, GJB3, GJB2, GJA5, GJA1, GHR, GDF1, GATA4, GPX4, GABRD, FZD2, KDSR, FLNB, FLNA, FLII, GLI3, RBPJ, FGFR1, LTBP3, NRAS, NPR2, NOTCH2, NOTCH1, NEK1, MAF, LTBP2, INPPL1, LIG4, LBR, KRAS, KCNJ2, ITGB6, INSR, FGFR2, FGF9, PAX3, BBS1, CHN1, CAMK2G, BRAF, BMP4, BGN, BBS4, ATRX, COL11A1, ATP7A, ATP6V1B2, RERE, ALX3, AKT1, AHSG, COL10A1, COL11A2, FGD1, EFNB1, GPC4, EXTL3, EXT1, EVC, ERF, MEGF8, DVL3, COMP, DVL1, SLC26A2, DHCR7, CTSK, NKX2-5, CSNK2A1, PAH, MEFV, PCNT, SDHB, TNNT3, TGFBR2, TCF12, TBX15, TBX1, MAP3K7, SOS2, SOS1, SMARCD2, SMARCA2, PCYT1A, SLC2A1, SKI, SHOX, SDHD, TRIO, TULP1, WNT5A, ARID1A, PAPSS2, MBTPS1, JAG1, KCNAB2, PPM1D, OFD1, SMC1A, ZIC1, KDM5C, LZTR1, MKKS, ALX1, SHOC2, KAT6A, SDHC, TMEM256-PLSCR3, RRAS, REV3L, PTPN11, MAP2K1, RPS6KA3, RAF1, RASA2, PPP3CA, RB1, DPF2, PPP2R1A, PPP1CB, PITX1, PTEN, RMRP, PIK3R1, PIK3CA, PDE6D, RPL10, RIT1, PDGFRB, PGM3, PTH, TBCEL, GHRH, FZD1, BDA1B, ASAH1, ADAMTS17, PHPT1, KCNB2, CRYGD, COL1A2, QRSL1, FOXC1, BRD2, PADI4, ACSL3, FRAS1, ADAMTS12, RTTN, SOX3, PARK7, SYK, PRPF31, GPC1, SACS, HLA-DRB1, HNRNPR, TBL1XR1
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Generalized Pustular Psoriasis
Wikipedia
PMID 21848462 . ^ Berki, DM; Liu, L; Choon, SE; David Burden, A; Griffiths, CEM; Navarini, AA; Tan, ES; Irvine, AD; Ranki, A; Ogo, T; Petrof, G; Mahil, SK; Duckworth, M; Allen, MH; Vito, P; Trembath, RC; McGrath, J; Smith, CH; Capon, F; Barker, JN (December 2015). ... PMID 26203641 . ^ Mahil, SK; Twelves, S; Farkas, K; Setta-Kaffetzi, N; Burden, AD; Gach, JE; Irvine, AD; Képíró, L; Mockenhaupt, M; Oon, HH; Pinner, J; Ranki, A; Seyger, MM; Soler-Palacin, P; Storan, ER; Tan, ES; Valeyrie-Allanore, L; Young, HS; Trembath, RC; Choon, SE; Szell, M; Bata-Csorgo, Z; Smith, CH; Di Meglio, P; Barker, JN; Capon, F (November 2016). ... Indian Journal of Dermatology, Venereology and Leprology . 75 (6): 638. doi : 10.4103/0378-6323.57743 . PMID 19915261 . ^ a b Zelickson BD, Muller SA (1991). "Generalized pustular psoriasis in childhood. ... Journal of the American Academy of Dermatology . 24 (2 Pt 1): 186–94. doi : 10.1016/0190-9622(91)70025-w . ... "The prognosis of generalized pustular psoriasis". Br. J. Dermatol . 85 (5): 407–11. doi : 10.1111/j.1365-2133.1971.tb14044.x .
- Pulmonary Capillary Hemangiomatosis Wikipedia
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Vertebral Hemangioma
Wikipedia
Case report, review of the literature, and management algorithm. Neurosurg Focus, 2005. 19 (3): p. E7. ^ a b Castel, E., et al., Acute spinal cord compression due to intraspinal bleeding from a vertebral hemangioma: two case-reports.
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Carey Fineman Ziter Syndrome
Wikipedia
Please help improve this article by adding citations to reliable sources . ... Am J Med Genet A 127A(3):291-293 ^ a b Di Gioia SA, Connors S, Matsunami N, Cannavino J, Rose MF, Gilette NM, Artoni P, de Macena Sobreira NL, Chan WM, Webb BD, Robson CD, Cheng L, Van Ryzin C, Ramirez-Martinez A, Mohassel P, Leppert M, Scholand MB, Grunseich C, Ferreira CR, Hartman T, Hayes IM, Morgan T, Markie DM, Fagiolini M, Swift A, Chines PS, Speck-Martins CE, Collins FS, Jabs EW, Bönnemann CG, Olson EN; Moebius Syndrome Research Consortium, Carey JC, Robertson SP, Manoli I, Engle EC.
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Iridoplegia
Wikipedia
Please help improve this article by adding citations to reliable sources . ... Archives of Disease in Childhood . 77 (1): 91–91. doi : 10.1136/adc.77.1.91a . PMC 1717230 .
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T Cell/histiocyte-Rich Large B-Cell Lymphoma
Wikipedia
"Regulatory Roles of MAPK Phosphatases in Cancer" . Immune Network . 16 (2): 85–98. doi : 10.4110/in.2016.16.2.85 . ... "SOCS1 in cancer: An oncogene and a tumor suppressor". Cytokine . 82 : 87–94. doi : 10.1016/j.cyto.2016.01.005 . ... "Diffuse large B-cell lymphoma: 2019 update on diagnosis, risk stratification, and treatment" . American Journal of Hematology . 94 (5): 604–616. doi : 10.1002/ajh.25460 . ... PMID 29988902 . ^ a b c Silva RNF, Mendonça EF, Batista AC, Alencar RCG, Mesquita RA, Costa NL (December 2019). ... PMID 28706431 . ^ Barut F, Kandemir NO, Gun BD, Ozdamar SO (July 2016). "T-cell/histiocyte-rich large B-cell lymphoma of stomach".
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Ischemia-Reperfusion Injury Of The Appendicular Musculoskeletal System
Wikipedia
"RGTA®-based matrix therapy – A new branch of regenerative medicine in locomotion". Joint Bone Spine . 84 (3): 283–292. doi : 10.1016/j.jbspin.2016.06.012 . ... "Improvement of cardiac stem cell sheet therapy for chronic ischemic injury by adding endothelial progenitor cell transplantation: analysis of layer-specific regional cardiac function". ... "Human relevance of pre-clinical studies in stem cell therapy: systematic review and meta-analysis of large animal models of ischaemic heart disease" . Cardiovasc Res . 91 (4): 649–58. doi : 10.1093/cvr/cvr113 . ... "Protection of mesenchymal stem cells on acute kidney injury" . Mol Med Rep . 9 (1): 91–96. doi : 10.3892/mmr.2013.1792 . ... "Cyclophilin D and myocardial ischemia-reperfusion injury: a fresh perspective". J Mol Cell Cardiol . 78 : 80–9. doi : 10.1016/j.yjmcc.2014.09.026 .
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Hypertrichosis Cubiti
Wikipedia
Hypertrichosis cubiti Specialty Dermatology Hypertrichosis cubiti (also known as " hairy elbow syndrome " [1] ) is a cutaneous condition characterized by multiple terminal hairs on both elbows in children. [1] Contents 1 Causes 2 Diagnosis 3 See also 4 References Causes [ edit ] One known cause of hypertrichosis cubiti is Wiedemann-Steiner syndrome . [2] [3] Diagnosis [ edit ] This section is empty. You can help by adding to it . ( July 2018 ) See also [ edit ] Hook nail List of cutaneous conditions References [ edit ] ^ a b Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... "De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome" . Am J Hum Genet . 91 : 358–64. doi : 10.1016/j.ajhg.2012.06.008 . ... American Journal of Human Genetics . 91 (2): 358–364. doi : 10.1016/j.ajhg.2012.06.008 .
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Substance Intoxication
Wikipedia
DSM-IV training guide . Psychology Press. pp. 80–. ISBN 978-0-87630-768-7 . Retrieved 27 April 2010 . ^ "Acute intoxication" . World Health Organization . Retrieved 2020-01-31 . ^ Johnson BD, BardhiF, Sifaneck SJ, Dunlap E (2005).
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Aortoesophageal Fistula
Wikipedia
Seminars in Vascular Surgery . 30 (2–3): 85–90. doi : 10.1053/j.semvascsurg.2017.10.005 . ... The American Journal of Medicine . 91 (3): 279–87. doi : 10.1016/0002-9343(91)90129-l . ... Gastrointestinal Endoscopy Clinics of North America . 26 (1): 99–118. doi : 10.1016/j.giec.2015.08.003 .
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Median Arcuate Ligament Syndrome
Wikipedia
. ^ Carbonell AM, Kercher KW, Heniford BT, Matthews BD (May 2005). "Multimedia article. Laparoscopic management of median arcuate ligament syndrome". ... J Vasc Interv Radiol . 6 (2): 165–74. doi : 10.1016/S1051-0443(95)71087-9 . PMID 7787348 . ^ Reilly LM, Ammar AD, Stoney RJ, Ehrenfeld WK (January 1985). "Late results following operative repair for celiac artery compression syndrome". J. Vasc. Surg . 2 (1): 79–91. doi : 10.1067/mva.1985.avs0020079 .
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Umbilical Cord Prolapse
Wikipedia
PMID 30174462 . ^ a b c d e f g h i Holbrook, BD; Phelan, ST (March 2013). "Umbilical cord prolapse". ... International Journal of Gynaecology and Obstetrics . 84 (2): 127–32. doi : 10.1016/s0020-7292(03)00333-3 . ... American Journal of Obstetrics and Gynecology . 170 (2): 613–8. doi : 10.1016/s0002-9378(94)70238-1 . PMID 8116723 . ^ a b c Murphy, DJ; MacKenzie, IZ (October 1995). ... American Journal of Perinatology . 16 (9): 479–84. doi : 10.1055/s-1999-6809 . PMID 10774764 . ^ a b c d e f g Lin, MG (April 2006). ... American Journal of Obstetrics and Gynecology . 165 (3): 654–7. doi : 10.1016/0002-9378(91)90303-9 . PMID 1892193 . ^ a b Koonings, PP; Paul, RH; Campbell, K (July 1990).
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Deafness, Autosomal Recessive 91
Omim
A number sign (#) is used with this entry because of evidence that autosomal recessive deafness-91 (DFNB91) is caused by homozygous mutation in the SERPINB6 gene (173321) on chromosome 6p25.
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Trigonocephaly
Wikipedia
Optima Grafische Communicatie. ISBN 978-90-8559-601-1 . ^ Wilkie, AO (1997). ... "Premature craniosynostosis: A common complication of juvenile thyrotoxicosis". The Journal of Pediatrics . 93 (2): 188–91. doi : 10.1016/S0022-3476(78)80493-4 . ... Plastic and Reconstructive Surgery . 80 (2): 195–212. doi : 10.1097/00006534-198708000-00006 . ... Plastic and Reconstructive Surgery . 119 (3): 977–84. doi : 10.1097/01.prs.0000252276.46113.ee . ... Plastic and Reconstructive Surgery . 93 (1): 16–24. doi : 10.1097/00006534-199401000-00003 .