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Molecular Genetics and Metabolism
|
June 3, 2004
Clinical, biochemical, and molecular diagnosis of a free sialic acid storage disease patient of moderate severity
Robert Kleta, Richard P Morse, Eduard Orvisky, et al.
Veterinary Pathology
|
September 1, 1987
Sphingomyelin lipidosis in a cat
H J Baker, P A Wood, D A Wenger, et al.
World Journal of Surgery
|
April 18, 2006
Laparoscopic and retroperitoneoscopic treatment of pheochromocytomas and retroperitoneal paragangliomas: results of 161 tumors in 126 patients
Martin K Walz, Piero F Alesina, Frank A Wenger, et al.
The Journal of Biological Chemistry
|
December 15, 1986
Type C Niemann-Pick disease. Abnormal metabolism of low density lipoprotein in homozygous and heterozygous fibroblasts
H S Kruth, M E Comly, J D Butler, et al.
Cytotherapy
|
August 16, 2015
Reprint of: Preclinical characterization of DUOC-01, a cell therapy product derived from banked umbilical cord blood for use as an adjuvant to umbilical cord blood transplantation for treatment of inherited metabolic diseases
Joanne Kurtzberg, Susan Buntz, Tracy Gentry, et al.
Malaria Journal
|
June 14, 2017
Effectiveness of reactive case detection for malaria elimination in three archetypical transmission settings: a modelling study
Jaline Gerardin, Caitlin A Bever, Daniel Bridenbecker, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Bone marrow transplantation for Niemann-Pick type IA disease
E Bayever, N Kamani, P Ferreira, et al.
Cytotherapy
|
March 16, 2015
Preclinical characterization of DUOC-01, a cell therapy product derived from banked umbilical cord blood for use as an adjuvant to umbilical cord blood transplantation for treatment of inherited metabolic diseases
Joanne Kurtzberg, Susan Buntz, Tracy Gentry, et al.
American Journal of Human Genetics
|
October 16, 1999
Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotype
G Millat, C Marçais, M A Rafi, et al.
Marine Pollution Bulletin
|
October 11, 2018
Fine sediment and particulate organic matter: A review and case study on ridge-to-reef transport, transformations, fates, and impacts on marine ecosystems
Z Bainbridge, S Lewis, R Bartley, et al.
Page
of 48
Search research articles
Search
Showing results (291-300 of 472) with videos related to
Sort By:
Page
of 48
Molecular Genetics and Metabolism
|
June 3, 2004
Clinical, biochemical, and molecular diagnosis of a free sialic acid storage disease patient of moderate severity
Robert Kleta, Richard P Morse, Eduard Orvisky, et al.
Veterinary Pathology
|
September 1, 1987
Sphingomyelin lipidosis in a cat
H J Baker, P A Wood, D A Wenger, et al.
World Journal of Surgery
|
April 18, 2006
Laparoscopic and retroperitoneoscopic treatment of pheochromocytomas and retroperitoneal paragangliomas: results of 161 tumors in 126 patients
Martin K Walz, Piero F Alesina, Frank A Wenger, et al.
The Journal of Biological Chemistry
|
December 15, 1986
Type C Niemann-Pick disease. Abnormal metabolism of low density lipoprotein in homozygous and heterozygous fibroblasts
H S Kruth, M E Comly, J D Butler, et al.
Cytotherapy
|
August 16, 2015
Reprint of: Preclinical characterization of DUOC-01, a cell therapy product derived from banked umbilical cord blood for use as an adjuvant to umbilical cord blood transplantation for treatment of inherited metabolic diseases
Joanne Kurtzberg, Susan Buntz, Tracy Gentry, et al.
Malaria Journal
|
June 14, 2017
Effectiveness of reactive case detection for malaria elimination in three archetypical transmission settings: a modelling study
Jaline Gerardin, Caitlin A Bever, Daniel Bridenbecker, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Bone marrow transplantation for Niemann-Pick type IA disease
E Bayever, N Kamani, P Ferreira, et al.
Cytotherapy
|
March 16, 2015
Preclinical characterization of DUOC-01, a cell therapy product derived from banked umbilical cord blood for use as an adjuvant to umbilical cord blood transplantation for treatment of inherited metabolic diseases
Joanne Kurtzberg, Susan Buntz, Tracy Gentry, et al.
American Journal of Human Genetics
|
October 16, 1999
Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotype
G Millat, C Marçais, M A Rafi, et al.
Marine Pollution Bulletin
|
October 11, 2018
Fine sediment and particulate organic matter: A review and case study on ridge-to-reef transport, transformations, fates, and impacts on marine ecosystems
Z Bainbridge, S Lewis, R Bartley, et al.
Page
of 48