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Annals of Burns and Fire Disasters|April 29, 2024

Nosocomial Infection Among Burn Patients Admitted to a Tertiary Care Hospital of Bangladesh: A Cross-Sectional StudyP K Dey, A Galib, A Sardar, 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 phenotypeG Millat, C Marçais, M A Rafi, et al.

Neuromuscular Disorders : NMD|June 14, 2002

Peripheral neuropathy with hypomyelinating features in adult-onset Krabbe's diseaseM Sabatelli, L Quaranta, F Madia, et al.

Laboratory Animal Science|March 25, 1999

Genetic galactocerebrosidase deficiency (globoid cell leukodystrophy, Krabbe disease) in rhesus monkeys (Macaca mulatta)G B Baskin, M Ratterree, B B Davison, et al.

Journal of Inherited Metabolic Disease|August 1, 1997

Prevalent mutations in the GALC gene of patients with Krabbe disease of Dutch and other European originW J Kleijer, J L Keulemans, M van der Kraan, et al.

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Showing results (31-40 of 35) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 35 results.

Annals of Burns and Fire Disasters|April 29, 2024

Nosocomial Infection Among Burn Patients Admitted to a Tertiary Care Hospital of Bangladesh: A Cross-Sectional StudyP K Dey, A Galib, A Sardar, 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 phenotypeG Millat, C Marçais, M A Rafi, et al.

Neuromuscular Disorders : NMD|June 14, 2002

Peripheral neuropathy with hypomyelinating features in adult-onset Krabbe's diseaseM Sabatelli, L Quaranta, F Madia, et al.

Laboratory Animal Science|March 25, 1999

Genetic galactocerebrosidase deficiency (globoid cell leukodystrophy, Krabbe disease) in rhesus monkeys (Macaca mulatta)G B Baskin, M Ratterree, B B Davison, et al.

Journal of Inherited Metabolic Disease|August 1, 1997

Prevalent mutations in the GALC gene of patients with Krabbe disease of Dutch and other European originW J Kleijer, J L Keulemans, M van der Kraan, et al.

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