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Skin Cancer In Horses
Wikipedia
XIV Congress. ^ a b c d e Valentine, Neoplasia , pg. 147. ^ a b Knottenbelt and McGarry, Sarcoids. , pg. 400. ^ a b c Valentine, "Neoplasia" pg. 149. ^ a b c d Torrontegui, B.O.; S. ... "Clinical and pathological epidemiology of the equine sarcoid in a referral population". Equine Veterinary Education . 6 (2): 85–88. doi : 10.1111/j.2042-3292.1994.tb01098.x . ^ a b Pascoe and Knottenbelt, Equine sarcoids. pg. 244 ^ Chambers, G; V. ... Retrieved August 11, 2011 . ^ Pascoe and Knottenbelt, Equine sarcoids. , pg. 247 ^ Pascoe and Knottenbelt. Equine sarcoids. , pg. 249. ^ a b c Pascoe and Knottenbelt. Equine sarcoids. pg. 251. ^ a b Knottenbelt, Derek C.; Donald F. ... Pg. 148 ^ Rooney and Robertson. [1] , pg. 305 ^ Fleury, Catherine; Frederic Bérard; Agnés Leblond; Christine Faure; Nathalie Ganem; Luc Thomas (February 2000).
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Inflammatory Bowel Disease 24
OMIM
They identified significantly associated loci at chromosome 20q13, rs2315008T and rs4809330A; P = 6.30 x 10(-8) and 6.95 x 10(-8), respectively, with an odds ratio of 0.74 for both. ... For the Wellcome Trust CD cohort, the odds ratio for each of these SNPs was 0.842 with a 95% confidence interval of 0.753 to 0.939; combined P values for both replication sets were 8.85 x 10(-15) for rs2315008 and 1.62 x 10(-14) for rs4809330. ... The mean +/- standard error of the mean (SEM) serum DCR3 concentration increased from 84 +/- 37 pg/ml in healthy controls to 4,333 +/- 1,637 pg/ml in individuals with IBD carrying the major allelic variants, and 11,793 +/- 2,452 pg/ml in individuals with IBD carrying the minor allelic variants, (P less than 0.05 for IBD vs control, and within IBD for major vs minor allelic variants). The UK IBD Genetics Consortium & the Wellcome Trust Case Control Consortium 2 (2009) performed a genomewide association scan in 2,361 ulcerative colitis (UC) cases and 5,417 controls followed by genotyping in an independent set of 2,321 UC cases and 4,818 controls, and found the strongest association (combined p = 8.5 x 10(-17)) at rs6017342, which maps within a recombination hotspot on 20q13 and is located 5 kb distal to the 3-prime UTR of the HNF4A gene (600281), within an expressed sequence tag (DB076868).
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Duodenal Ulcer, Hyperpepsinogenemic I
OMIM
Human gastric mucosa contains 2 immunochemically distinct types of pepsinogens, I and II. Only pepsinogen I (PG I) is derived exclusively from the chief cells in the oxyntic glands of the gastric body and fundus. ... Rotter et al. (1979) found autosomal dominant transmission of elevated serum PG I level in 2 large families with a prominent history of duodenal ulcer. An elevated PG I level identified genetically susceptible but clinically normal persons. About half of sibships with 2 or more cases of duodenal ulcer were found to segregate for high serum PG I.
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Muscardine
Wikipedia
Over 10 Aspergillus species can cause the disease, such as A. flavus and A. tamari . ... FAO. 1991. pg. 37. ^ Mahr, S. Know Your Friends: The Entomopathogen Beauveria bassiana . Midwest Biological Control News October, 1997. Volume IV, Number 10. ^ Wang, C. and Y. Xia. Cover photo. ... Insect Pathology . Academic Press. 2012. pg. 433. ^ Chernin, L., et al. (1997). ... Two Muscardine fungi pathogenic to Diaprepes abbreviatus . The Florida Entomologist 55(2) 117-120. ^ Vyas, R. V., et al. (1992).
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Fear Of Medical Procedures
Wikipedia
No wonder half of all children from ages of 2 to 10 show evidence of distress—from bed-wetting to nightmares—for at least two weeks after their operation. ... ISBN 0-8261-1427-X . ^ a b c d Specific Phobias: Clinical Applications of Evidence-Based Psychotherapy pg 5 ^ Diagnostic and Statistical Manual for Mental Disorders (DSM-IV; American Psychiatric Association, 1994) ^ Phobic Disorders and Panic in Adults: A guide to Assessment and Treatment pg 79 ^ Fears, Phobias, and Rituals: Panic, Anxiety and their Disorders pg 376 ^ Phobic Disorders and Panic in Adults: A guide to Assessment and Treatment pg 82 ^ a b Fears, Phobias, and Rituals: Panic, Anxiety and their Disorders pg 377 ^ Fears, Phobias, and Rituals: Panic, Anxiety and their Disorders pg 378 ^ Phobic Disorders and Panic in Adults: A guide to Assessment and Treatment pg 84 ^ Phobic Disorders and Panic in Adults: A guide to Assessment and Treatment pg 98-102 ^ Schmid, Markus; Wolf, Robert C; Freudenmann, Roland W; Schönfeldt-Lecuona, Carlos (2009-11-18). ... USA Today Magazine, 01617389, Feb96, Vol. 124, Issue 2609 ^ a b Fear of Cataract Operation in Aged Persons, Ritva Fagerstro:m Psychological Reports, 1993, 72, 1339-1346, pg.1339 ^ Fear of Cataract Operation in Aged Persons, Ritva Fagerstro:m Psychological Reports, 1993, 72, 1339-1346pg.1339 (Paddison, Strain, Strain & Strain, 1989) ^ Fear of Cataract Operation in Aged Persons, Ritva Fagerstro:m Psychological Reports, 1993, 72, 1339- 1346, pg. 1340 ^ Fear of Cataract Operation in Aged Persons, Ritva Fagerstro:m Psychological Reports, 1993, 72, 1339-1346, pg. 1342 ^ a b Fear of Cataract Operation in Aged Persons, Ritva Fagerstro:m Psychological Reports, 1993, 72, 1339-1349, pg. 1344 ^ Fear of Cataract Operation in Aged Persons, Ritva Fagerstro:m Psychological Reports, 1993, 72, 1339-1349, pg. 1345 ^ a b c Dental fear: Comparisons Between Younger and Older Adults, M. Michelle Rowe, PhD American Journal of Health Studies: 20(4) 2005 pg. 219-224 ^ a b c d Dental Fear in Children- a proposed model, H.R. ... "Needle Phobia - A Neglected Diagnosis". Journal of Family Practice . 41 (2): 169–175. PMID 7636457 . Lountzis and Rahman 359 (2): 177, July 10, 2008 The New England Journal of Medicine Further reading [ edit ] Margaret S.
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Purple Glove Syndrome
Wikipedia
Purple glove syndrome Specialty Dermatology Purple glove syndrome (PGS) is a poorly understood skin disease in which the extremities become swollen , discoloured and painful. [1] PGS is potentially serious, and may require amputation . PGS is most common among elderly patients and those receiving multiple large intravenous doses of the epilepsy drug phenytoin . [2] Compartment syndrome is a complication of PGS. Contents 1 Cause 2 Diagnosis 3 Treatment 4 References 5 External links Cause [ edit ] Purple glove syndrome is caused by the intravenous anticonvulsant phenytoin.
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Pygmy
OMIM
By in vitro analysis of 6 cell lines from Pygmies, Hattori et al. (1996) determined that the Pygmy-derived cells showed markedly decreased cell surface expression of IGF1 receptors (IGF1R; 147370) compared to controls, although the affinity of IGF1 binding to the receptor was similar in the 2 cell lines. There was a substantially decreased level of IGF1 receptor mRNA (2 to 13% of control) in the Pygmy cells, with a normal mRNA half-life. ... Hattori et al. (1996) detected no pathogenic mutations by sequence analysis of IGF1R cDNA from transformed T lymphocyte lines derived from Pygmies. In 2 non-Pygmy patients with short stature and IGF1 resistance (see 270450) due to decreased number or function of cell surface IGF1 receptors, Abuzzahab et al. (2003) identified mutations in the IGF1R gene (147370.0001-147370.0003). ... Animal Model The mouse mutation called pygmy (pg), a recessive that maps to mouse chromosome 10, has only similarity of name to the human condition. In pg mice, Xiang et al. (1990) identified a mutation in the pg gene (HMGA2; 600698).
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Whale Oil
Wikipedia
Whale oil is mainly composed of triglycerides [10] (molecules of fatty acids attached to a glycerol molecule). ... Archived from the original on 2019-10-06 . Retrieved 2019-10-07 . Then in 1846, a Nova Scotian physician and geologist named Abraham Gesner invented kerosene. ... A Practical Treatise on Friction, Lubrication, Fats and Oils . pg 23 ^ Frank Sims (1999). Engineering Formulas Interactive: Conversions, Definitions, and Tables . pg 132 ^ J. ... Goldsmith (1921). Table of Refractive Indices . pg 259 ^ Video on YouTube ^ Wilson Heflin (2004). Herman Melville's Whaling Years . pg 232 ^ "Thefreemanonline.org" . www.thefreemanonline.org . ^ "The "Whale Oil Myth " " .
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Abarognosis
Wikipedia
Abarognosis Other names Baragnosis, baroagnosis [1] Abarognosis () is type of cortical sensory defect [2] consisting of a loss of barognosis , the ability to detect the weight of an object held in the hand or to tell the difference in weight between two objects, [3] or more succinctly "Loss of the ability to sense weight". [4] This deficit may be caused by damage to the parietal lobe . [5] The term is from Greek "a" not, "baros" weight, "gnosis" knowledge. Contents 1 References 1.1 Notes 1.2 Sources 2 External links References [ edit ] Look up abarognosis in Wiktionary, the free dictionary. Notes [ edit ] ^ Dorland 2011, baragnosis ^ Black 1995, pg. 14 ^ abarognosis , Drugs.com , retrieved 2013-03-21 ^ "abarognosis" , The American Heritage® Stedman's Medical Dictionary , Houghton Mifflin , retrieved 2013-03-21 ^ Campbell 2012, pg. 554 Sources [ edit ] Black, Peter McLaren; Rossitch, Eugene (1995), "Neurological Diagnosis" , Neurosurgery: An Introductory Text (Google eBook), Oxford University Press , ISBN 9780195044492 , retrieved 2013-02-21 Buck, Carol J. (2013), "Section Index to Diseases and Injuries" , 2013 ICD-9-CM for Physicians (Google preview), Vol. 2 (Professional ed.), Elsevier Health Sciences , ISBN 9781455775033 , retrieved 2013-03-21 Campbell, William W. (2012), "36: Sensory Localization" , DeJong's The Neurologic Examination (Google eBook) (7th ed.), Lippincott Williams & Wilkins , ISBN 9781469817521 , retrieved 2013-03-21 Dorland (2011), Dorland's Illustrated Medical Dictionary (Google eBook) (32nd ed.), Elsevier Health Sciences, ISBN 9781455709854 , retrieved 2013-03-21 External links [ edit ] Classification D ICD - 9-CM : 781.99
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Oslam Syndrome
Wikipedia
OSLAM syndrome was recognised and described by Mulvilhill et al. as a syndrome that increases susceptibility to tumours and is characterised by an impaired regulation of bone and marrow development. [1] [2] Individuals with OSLAM syndrome have an elevated risk of bone cancer, limb abnormalities, and enlarged red blood cells. Contents 1 Signs and symptoms 2 Diagnosis 3 Treatment 4 See also 5 References 6 External links Signs and symptoms [ edit ] Bone cancer Curved fifth fingers (clinodactyly) with brachymesophalangy (shortened phalanges of the toes and/or fingers (digits)) Absence of one digital ray of the foot (a digit and corresponding metacarpal or metatarsal bone) Bilateral radioulnar synostosis Enlarged red blood cells Dental decay Short stature Diagnosis [ edit ] This section is empty. ... Molecular Mechanisms of Cancer , Springer, pg. 558. External links [ edit ] Classification D ICD - 10 : C41.9 OMIM : 165660 MeSH : C537138 External resources Orphanet : 2760 This genetic disorder article is a stub .
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Pemphigoid Gestationis
Orphanet
Clinical description Pemphigoid gestationis (PG) Pemphoid gestationis (PG) typically presents during the second or third trimesters, although onset during the first trimester and postpartum is possible. ... Recurrence in subsequent pregnancies is common (35-50%), and is typically more severe with earlier onset. PG is associated with the autoimmune Graves' disease in the mother. There is an increased risk of small-for-gestational-age baby, premature birth, and development of mild, self-limiting skin lesions in the neonate (10-11%). PG can be associated with the autoimmune Graves' disease in the mother. ... PG is strongly associated with maternal MHC class II antigens haplotypes HLA-DR3 and HLA-DR4. Diagnostic methods Clinical and histological features are not specific to PG; therefore, additional tests are required for diagnosis.
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Ménétrier's Disease
Wikipedia
The disorder is associated with excessive secretion of transforming growth factor alpha (TGF-α). [1] It is named after a French physician Pierre Eugène Ménétrier , 1859–1935. Contents 1 Signs and symptoms 2 Cause 3 Pathology 4 Diagnosis 5 Treatment 6 Epidemiology 7 References 8 External links Signs and symptoms [ edit ] Individuals with the disease present with upper abdominal pain (epigastric), at times accompanied by nausea, vomiting, loss of appetite , edema , weakness, and weight loss. ... Diffuse or patchy glandular atrophy, evident as hypoplasia of parietal and chief cells, is typical. [4] Although ICD-10 classifies it under "Other gastritis" ( K29.6 ), and the lamina propria may contain mild chronic inflammatory infiltrate, Ménétrier disease is not considered a form of gastritis. [3] It is rather considered as one of the two most well understood hypertrophic gastropathies; the other being Zollinger–Ellison syndrome . [4] Diagnosis [ edit ] CT abdomen, coronal section, showing characteristic large rugal folds in the stomach. ... Other possible causes (eg differential diagnosis) of large folds within the stomach include: Zollinger-Ellison syndrome, cancer , infection ( cytomegalovirus /CMV, histoplasmosis , syphilis ), and infiltrative disorders such as sarcoidosis . [3] Treatment [ edit ] Cetuximab is the first-line therapy for Ménétrier disease. [2] Cetuximab is a monoclonal antibody against epidermal growth factor receptor (EGFR), and has been shown to be effective in treating Ménétrier disease. [6] Several medications have been used in the treatment of the condition, with variable efficacy. ... Epidemiology [ edit ] The average age of onset is 40 to 60 years, and men are affected more often than women. [2] Risk of gastric adenocarcinoma is increased in adults with Ménétrier disease. [4] [5] References [ edit ] ^ a b Coffey RJ; et al. (2007). ... ISBN 978-0071802154 . ^ a b c d e Harrison's Principle of Internal Medicine, 18e, pg 2459 ^ a b c d Robbins and Cotran, Pathological Basis of Disease, 8e, pg 782 ^ a b c d Kumar et al., Pathologic Basis of Disease, 2e , pg 768 ^ Burdick JS, Chung E, Tanner G, et al.
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Narcolepsy Type 1
Orphanet
Clinical description The age of onset varies between 10 and 30 years old and symptoms are lifelong. The average time between the age of appearance of the symptoms and the diagnosis is still very long, 10 years. Other, non specific, clinical signs include hypnagogic hallucinations, sleep paralysis, disturbed nocturnal sleep, and weight gain, especially in children. ... The presence of low hypocretin-1 levels (<110 pg/ml) in the cerebrospinal fluid can confirm the diagnosis with an excellent sensibility and specificity. ... In absence of typical cataplexy, other causes of sleepiness must be considered, such as chronic insufficient sleep, idiopathic hypersomnia or narcolepsy without cataplexy, now called narcolepsy type 2. Genetic counseling Rare familial cases have been reported (<2%); however the mode of inheritance is unclear.HLA-DQB1, HCRT, HLA-DRB1, MOG, HCRTR2, P2RY11, CTSH, ZNF365, CPT1B, CHKB, TRA, EIF3G, TNFSF4, TAC1, TRH, PENK, SOCS2, HLA-DQA1, DNMT1, PPAN, PPAN-P2RY11, CHKB-CPT1B, MAP3K7, NOTCH4, HLA-DQA2, NRXN1, ANO3, TMEM108, TBL1XR1, COLGALT1, ZYG11B, GALNT14, MMP26, MRPL24, JPH1, NUP37, FSTL5, SLC28A3, CA10, LYRM4, ADAMTSL3, TENM2, LRRC7, WDR48, DPP10, LRRN1, VAT1L, LRRC4C, ASIC2, RBFOX1, BTNL2, OXR1, AGTR1, CACNG2, TSBP1, NPFFR2, TCERG1, POLI, KLF12, MRAS, DENND3, ATF6, PALLD, SWAP70, TMEM131L, MTUS2, SRGAP2, DDAH1, KCNE4, TANC2, AK5, PDE7B, BBS9, RBMS3, REM1, NXPH1, NOX4, PHF20, DYNC2LI1, FHOD3, CDKAL1, ZNF385D, SERAC1, CCDC68, LINC00687, ZEB1-AS1, FAM171A1, NT5DC1, SDK1, LINC01619, HS6ST3, SUMF1, IQCM, HLA-F-AS1, NKAIN3, FREM2, RPS10P7, CATSPER4, SHC4, DCDC2C, GLIS3, MAPT-AS1, C9orf92, LINC00861, ATP5MC1P6, HOXD-AS2, SPRY4-AS1, LINC01847, LINC01687, LINC01182, TSBP1-AS1, LINC01500, LINC02336, LINC01839, LINC02511, CEP112, TOGARAM2, CYB5B, ANTXR2, ITCH, ACSS1, PYROXD2, ELMO1, ERI1, ALKBH8, SNX29, SHKBP1, FOXP2, PIK3IP1, TRIM9, CSMD3, TMEM132B, C8orf34, PIK3AP1, MDGA2, AGBL1, HSD3BP4, RBM45, EGFLAM, HINT3, UBXN2B, UNC5D, FAUP1, SUN5, FRMPD2, PLB1, LINC00691, NKAIN2, LINC00964, RAD50, FRY, LINC02248, SFRP1, PSMA5, PSMB9, EPHB1, EDNRA, RIT2, RYR2, DPYD, DPP6, PRCP, DNAH8, SLC18A2, STIM1, TAP1, TAP2, TF, TIAM1, FGF10, PPARA, MCC, GRM5, HLA-F, HLA-DRB9, NFRKB, HLA-DRA, HLA-DQB2, HLA-DOB, GRM8, GRID1, GPC5, GNAO1, GABRG3, FXN, FOLR1, PDE4B, FHIT, SERPINB5, TJP1, ITGA3, DHODH, CTNND2, RNGTT, KALRN, BLMH, BCR, MAGI1, DLGAP2, DLGAP1, NDST3, AKAP6, ATG5, ATP2B2, ASTN1, MICAL2, HDAC9, JAKMIP2, NOL4, DCHS1, BARX2, CTNNA2, SERPING1, H2AC6, SLC14A2, EPM2A, CDK8, CENPC, DAP3, VDR, CILP, VAV2, COL14A1, VAV1, TNF, COMT, HLA-DRB5, HRH3, CCR3, P2RX5-TAX1BP3, ATXN3, P2RY2, P2RY1, P2RX5, P2RX4, TNFRSF1B, P2RX3, P2RX1, TRIB2, P2RX7, P2RX2, P2RX6, LEP, HCRTR1, PSG5, HLA-A, PICSAR, HLA-DPB1, MX2, NFATC2, TAAR1, TNFRSF1A, MIR30C2, SLC6A2, LINC00163, SLC6A3, MIR320A, SKOR1, ZGLP1, MIR130A, MIR30C1, TRAC, CSF3, CRP, TRAJ60, TRAV29DV5, MIR4455, GDNF-AS1, CCR1, SLC17A5, FGF21, CD40LG, SMUG1, CLOCK, ABCG1, SALL4, CIITA, RANGAP1, NAA50, ABCC9, CXCL8, IFNG, IFNA17, IFNA13, IFNA2, IFNA1, IFN1@, HTR2A, MS, FAM3D, CD200R1, HLA-DRB4, HDC, PTPRD, EHMT1, GLP1R, FBXO15, GHRH, GH1, GDNF, GCG, GAD2, MAOA, PRKN, PDYN, POLE, QRFP, CCS
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Hughes–stovin Syndrome
Wikipedia
Radiological features are similar to those of Behçet's disease. [2] Contents 1 Signs and symptoms 2 Diagnosis 3 Management 4 References 5 External links Signs and symptoms [ edit ] Multiple pulmonary aneurysms [3] Peripheral venous thrombosis [3] Recurrent fever [3] Chills [3] Hemoptysis [3] Cough [3] Diagnosis [ edit ] There is no rigid set of diagnostic criteria for Hughes-Stovin. ... According to the Orphanet Journal , treatments, including ventilator , surgery and transcatheter arterial embolization are also used. [5] References [ edit ] ^ Hughes, JP; Stovin, PG (January 1959). "Segmental pulmonary artery aneurysms with peripheral venous thrombosis". ... "Hughes-Stovin Syndrome: a case report and review of the literature" . Cases J . 2 : 98. doi : 10.1186/1757-1626-2-98 . ... QJM: An International Journal of Medicine . 111 (10): 729–730. doi : 10.1093/qjmed/hcy110 . ... External links [ edit ] Classification D ICD - 10 : I28.8 External resources Orphanet : 228116 This article about a disease of the blood or immune system is a stub .
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Odynorgasmia
Wikipedia
Causes include infections associated with urethritis , prostatitis , epididymitis , as well as use of anti-depressants . [1] [2] References [ edit ] ^ Richard Balon, R. Taylor Segraves, Handbook of sexual dysfunction , Informa Healthcare; 1 edition (April 14, 2005), pg 241 ^ Donnellan P, Breathnach O, Crown JP (April 2001). ... Scandinavian Journal of Urology and Nephrology . 35 (2): 158. doi : 10.1080/003655901750170687 .
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Zollinger-Ellison Syndrome
Orphanet
Epidemiology Annual incidence is estimated at 1-2 cases per million. The condition is slightly more common in females than males (sex ratio of 1.3:1). ... Elevated fasting serum gastrin (FSG) levels are almost invariably present. FSG levels 10 times higher than normal and a gastric pH of <2 confirm the diagnosis. If the FSG level is elevated less than 10 fold and the gastric pH is <2, secretin stimulation (abnormal: increase >120 pg/ML) and basal acid (abnormal: >15 mEq/hr-basal) tests need to be done. ... Prognosis In the absence of liver metastases, the prognosis is favorable (10-year survival rate of 90-100%). Patients with liver metastases (65-75% of patients) have a 10-year survival rate of 20-40%. Patients with MEN1 are rarely cured surgically due to the presence of multiple tumors and lymph node metastases, however, only 15% pursue an aggressive course and 10 year survival is 80-98%.MEN1, GAST, CHGA, SST, SCT, CDKN2A, ACTB, SCTR, GRPR, GRP, ERBB2, POTEF, CASR, MET, NMBR, POMC, PYGM, S100B, BBS2, ATP4A, ATP12A, SSTR5, TCF3, TNFRSF1B, TP53, VIP, KHSRP, PSIP1, SIGLEC7, NMB, CUX1, EGF, SMAD4, EGFR, CDKN2D, CDKN2B, GFAP, GH1, FFAR1, CDH1, CD44, HCLS1, HGF, APC, IGF1, IGF1R, IGFBP1, IL2RB, HRH2
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Antiphospholipid Syndrome
Wikipedia
Archives of Pathology & Laboratory Medicine . 126 (11): 1424–9. doi : 10.1043/0003-9985(2002)126<1424:AA>2.0.CO;2 (inactive 2020-12-22). PMID 12421152 . ... The American Journal of the Medical Sciences . 316 (2): 142–51. doi : 10.1097/00000441-199808000-00009 . ... PMID 1329261 . ^ a b Miyakis S, Lockshin MD, Atsumi T, Branch DW, Brey RL, Cervera R, Derksen RH, DE Groot PG, Koike T, Meroni PL, Reber G, Shoenfeld Y, Tincani A, Vlachoyiannopoulos PG, Krilis SA (February 2006). ... Lancet . 376 (9751): 1498–509. doi : 10.1016/S0140-6736(10)60709-X . hdl : 2318/1609788 . PMID 20822807 . ... "Antiphospholipid Syndrome Clinical Research Task Force Report". Lupus . 20 (2): 219–224. doi : 10.1177/0961203310395053 .APOH, PPARG, FRMD4A, TSHR, F5, F3, SYCP2L, F2, PTPRO, GPI, ANXA5, TLR4, SH2B2, KLK3, ANXA2, TNF, AGER, CPB2, MTOR, MTHFR, F10, PLG, HT, TFPI, PLAT, SELPLG, ACR, SERPINE1, MOK, LRP8, VWF, HMGB1, VIM, SELP, RAB4A, CCL2, CXCL12, ATXN2, RO60, S100A10, TRIM21, ABCA1, SSB, THBD, TNFRSF1B, NR1I2, ADIPOQ, SH2B3, PROCR, ADAMTS13, TREX1, PTPN22, FOXP3, SLC52A1, IL21, ANXA8, ANXA8L1, PROS1, NOS3, PON1, PLSCR1, HLA-DPB1, GP1BA, GCY, FGA, FCGR2A, F2RL1, EMD, EDN1, DECR1, CRP, CD36, CD1D, CALR, B2M, SERPINC1, AQP4, AMH, HLA-DRB1, HRES1, IDS, MBL2, PF4, PC, SERPINB2, TNFRSF11B, MYD88, MSN, MPL, LPA, IFNG, LGALS9, LCT, CXCL10, CXCL8, IL1B, IGFBP1, IGF1, C20orf181
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Pleomorphic Anaplastic Neuroblastoma
Wikipedia
Pleomorphic anaplastic neuroblastoma (PAN) is a striking aspect of neuroblastoma first described by Cozzutto and Carbone in 1988. [1] Another case was thereafter reported by Cowan, et al. with cytogenetic and immunohistological analysis in a 28-year-old man. [2] The case described by Navarro, et al. showed MYCN amplification (more than 10 copies) and a 1p36 deletion as measured with FISH in 13% of cells. [3] Additionally there was a main cell population with a DNA index of 2 indicating a tetraploid DNA content and a high expression of MIBI (Ki-67), bel 2, p53, and P-glycoprotein , either correlated with rapid progression of disease. ... Letter to the editor. Arch Pathol Lab Med 113:9-10. ^ Abramowsky CR, Katzenstein HM, Alvarado CS, Shehata BM (2009). ... Recommendations by the International Neuroblastoma Pathology Committee. Cancer 86(2):349-363. ^ Tornòczky T, Kàlmàn E, Kajtàr PG, Nyàri T, Pearson AD, Tweddle DA, Board J, Shimada H (2004) Large cell neuroblastoma. A distinctive phenotype of neuroblastoma with aggressive clinical behavior. Cancer 100(2):390-397. Shimada H, Ambros IM, Dehner LP, Hata J, Joshi VV, Roald B (1999). ... Recommendations by the International Neuroblastoma Pathology Committee. Cancer 86(2) 349-363.
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Mixed Transcortical Aphasia
Wikipedia
Responsive Speech ("What do you write with?") 2. Spontaneous Speech a. Conversational questions b. ... Retrieved March 22, 2015, from: https://books.google.com/books?id=wM9sBQAAQBAJ&pg=PA198 ^ Nussbaum, P. (1997). Handbook of neuropsychology and aging (p.305). ... Retrieved March 22, 2015 from https://books.google.com/books?id=QxR6EaATaUwC&pg=PA545 ^ LaPointe, L (2005). Aphasia and related neurogenic language disorders (3rd ed., p.117). ... Retrieved March 22, 2015, from https://books.google.com/books?id=PgRbFxayeQwC&pg=PA181 ^ a b LaPointe, L (2005). Aphasia and related neurogenic language disorders (3rd ed., p.117). ... Retrieved March 22, 2015, from https://books.google.com/books?id=PgRbFxayeQwC&pg=PA181 ^ a b c d e f g Farias, et al, (2006).
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Merciful Anosmia
Wikipedia
Merciful anosmia is a condition in which the person is unaware of a foul smell emanating from his own nose . [1] [2] This condition is seen in atrophic rhinitis . ... ISBN 9788131223642 . ^ "Atrophic rhinitis" . PG Blazer . Retrieved 14 March 2013 .
