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Clinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1989
Phosphatidylcholine storage in mucolipidosis IVR Bargal, G BachJournal of Inherited Metabolic Disease|January 1, 1988
Phospholipids accumulation in mucolipidosis IV cultured fibroblastsR Bargal, G BachJournal of Inherited Metabolic Disease|November 5, 1997
Mucolipidosis type IV: abnormal transport of lipids to lysosomesR Bargal, G BachNeuropediatrics|October 9, 2002
Mucolipidosis IV: novel mutation and diverse ultrastructural spectrum in the skinR Bargal, H H Goebel, E Latta, et al.Prenatal Diagnosis|December 1, 1992
Mucolipidosis type IV: accumulation of phospholipids and gangliosides in cultured amniotic cells. A tool for prenatal diagnosisM Zeigler, R Bargal, V Suri, et al.Human Mutation|March 1, 2000
Niemann Pick Disease type A in Israeli Arabs: 677delT, a common novel single mutation. Mutations in brief no. 161. OnlineI Gluck, M Zeigler, R Bargal, et al.European Journal of Human Genetics : EJHG|June 3, 1999
Mucolipidosis type IV: the origin of the disease in the Ashkenazi Jewish populationA Raas-Rothschild, R Bargal, S DellaPergola, et al.Prenatal Diagnosis|March 11, 2003
Mucolipidosis III type C: first-trimester biochemical and molecular prenatal diagnosisT C Falik-Zaccai, M Zeigler, R Bargal, et al.Nature Genetics|September 6, 2000
Identification of the gene causing mucolipidosis type IVR Bargal, N Avidan, E Ben-Asher, et al.Human Mutation|April 24, 2001
Mucolipidosis type IV: novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish populationR Bargal, N Avidan, T Olender, et al.Pageof 25