Mohammad A. Rafi

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

Gilles Millat, Christophe Marçais, Mohammad A. Rafi et al. · The American Journal of Human Genetics · 1999 · 204 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +12

Cloning and expression cDNA encoding human galactocerebrosidase, the enzyme deficient in globoid cell leukodystrophy

Yue Qun Chen, Mohammad A. Rafi, Gregory de Gala et al. · Human Molecular Genetics · 1993 · 150 citations

PET Imaging of Bacterial Infections with Fluorine‐18‐Labeled Maltohexaose

Xinghai Ning, Wonewoo Seo, Seungjun Lee et al. · Angewandte Chemie International Edition · 2014 · 141 citations · Full text

Positron Emission Tomography, Antimicrobial Susceptibility, Health Sciences +12

Extended Normal Life After AAVrh10-mediated Gene Therapy in the Mouse Model of Krabbe Disease

Mohammad A. Rafi, Han Zhi Rao, Paola Luzi et al. · Molecular Therapy · 2012 · 113 citations · Full text

AAV-Mediated expression of galactocerebrosidase in brain results in attenuated symptoms and extended life span in murine models of globoid cell leukodystrophy

Mohammad A. Rafi, Han Zhi Rao, Marco A. Passini et al. · Molecular Therapy · 2005 · 110 citations · Full text