These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
110 related articles for article (PubMed ID: 22097942)
1. Education and imaging. Hepatobiliary and pancreatic: Niemann-Pick disease. Hasosah M; Satti M J Gastroenterol Hepatol; 2011 Dec; 26(12):1813. PubMed ID: 22097942 [No Abstract] [Full Text] [Related]
2. Infant with type A Niemann Pick disease and undetectable Niemann Pick cells in bone marrow. Mukherjee SB; Pandey M; Kapoor S; Priya TP Indian Pediatr; 2012 Jun; 49(6):490-2. PubMed ID: 22796693 [TBL] [Abstract][Full Text] [Related]
4. R542X mutation in SMPD1 gene: genetically novel mutation with phenotypic features intermediate between type A and type B Niemann-Pick disease. Aneja A; Sharma A; Dalal A; Sondhi V BMJ Case Rep; 2012 Nov; 2012():. PubMed ID: 23188845 [TBL] [Abstract][Full Text] [Related]
5. Hepatobiliary and pancreatic: a diabetic woman with chronic liver disease unrelated to a virus or alcohol. J Gastroenterol Hepatol; 2003 Mar; 18(3):344, 350. PubMed ID: 12603539 [No Abstract] [Full Text] [Related]
6. Deep sequencing of SMPD1 gene revealed a heterozygous frameshift mutation (p.Ser192Alafs) in a Palestinian infant with Niemann-Pick disease type A: a case report. Nasereddin A; Ereqat S J Med Case Rep; 2018 Sep; 12(1):272. PubMed ID: 30223864 [TBL] [Abstract][Full Text] [Related]
7. Alleged Detrimental Mutations in the SMPD1 Gene in Patients with Niemann-Pick Disease. Rhein C; Mühle C; Kornhuber J; Reichel M Int J Mol Sci; 2015 Jun; 16(6):13649-52. PubMed ID: 26084044 [TBL] [Abstract][Full Text] [Related]
8. Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population. Cerón-Rodríguez M; Vázquez-Martínez ER; García-Delgado C; Ortega-Vázquez A; Valencia-Mayoral P; Ramírez-Devars L; Arias-Villegas C; Monroy-Muñoz IE; López M; Cervantes A; Cerbón M; Morán-Barroso VF Ann Hepatol; 2019; 18(4):613-619. PubMed ID: 31122880 [TBL] [Abstract][Full Text] [Related]
9. Serum liver enzymes--should we count on them? Oren R Liver Int; 2014 Feb; 34(2):171-3. PubMed ID: 24164713 [No Abstract] [Full Text] [Related]
10. SMPD1 Mutation Update: Database and Comprehensive Analysis of Published and Novel Variants. Zampieri S; Filocamo M; Pianta A; Lualdi S; Gort L; Coll MJ; Sinnott R; Geberhiwot T; Bembi B; Dardis A Hum Mutat; 2016 Feb; 37(2):139-47. PubMed ID: 26499107 [TBL] [Abstract][Full Text] [Related]
11. Acid sphingomyelinase (Asm) deficiency patients in The Netherlands and Belgium: disease spectrum and natural course in attenuated patients. Hollak CE; de Sonnaville ES; Cassiman D; Linthorst GE; Groener JE; Morava E; Wevers RA; Mannens M; Aerts JM; Meersseman W; Akkerman E; Niezen-Koning KE; Mulder MF; Visser G; Wijburg FA; Lefeber D; Poorthuis BJ Mol Genet Metab; 2012 Nov; 107(3):526-33. PubMed ID: 22818240 [TBL] [Abstract][Full Text] [Related]
13. Seven novel mutations of the SMPD1 gene in four Chinese patients with Niemann-Pick disease type A and prenatal diagnosis for four fetuses. Ding Y; Li X; Liu Y; Hua Y; Song J; Wang L; Li M; Qin Y; Yang Y Eur J Med Genet; 2016 Apr; 59(4):263-8. PubMed ID: 26851525 [TBL] [Abstract][Full Text] [Related]
14. Interstitial Lung Disease Associated with Adult Niemann-Pick Disease Type B. Chebib N; Thivolet-Bejui F; Cottin V Respiration; 2017; 94(2):237-238. PubMed ID: 28601876 [No Abstract] [Full Text] [Related]
16. [Usefulness of gamma-glutamyltransferase in alcoholic hepatotoxicity]. Casacchia M; Meco G; Carchedi F; Paris L; Avoli M; Cerbo R Boll Soc Ital Biol Sper; 1978 Feb; 53(24):2493-6. PubMed ID: 25074 [No Abstract] [Full Text] [Related]
17. An induced pluripotent stem cell line (TRNDi009-C) from a Niemann-Pick disease type A patient carrying a heterozygous p.L302P (c.905 T>C) mutation in the SMPD1 gene. Baskfield A; Li R; Beers J; Zou J; Liu C; Zheng W Stem Cell Res; 2019 Jul; 38():101461. PubMed ID: 31132580 [TBL] [Abstract][Full Text] [Related]
18. Hepatobiliary and Pancreatic: Mauriac syndrome: A rare cause of elevated liver enzymes. Khan F; Parikh MP; McCullough AJ J Gastroenterol Hepatol; 2019 Feb; 34(2):313. PubMed ID: 30112859 [No Abstract] [Full Text] [Related]
19. A 51Cr release cytotoxicity assay for use with human intrahepatic biliary epithelial cells. Ayres RC; Shaw J; Mills CO; Coleman R; Neuberger JM J Immunol Methods; 1991 Jul; 141(1):117-22. PubMed ID: 1677952 [TBL] [Abstract][Full Text] [Related]
20. [Type A Niemann-Pick disease in a female Arab infant]. Zelikovic I; Nitzan M; Zitman D; Klibansky C Harefuah; 1977 Nov; 93(9):239-42. PubMed ID: 598759 [No Abstract] [Full Text] [Related] [Next] [New Search]