D. Germain
Annals of Internal Medicine · with Barranger · 2003–2010
A researcher in the Science corpus: 2 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Papers from D. Germain's perspective
Ordered by how strongly the researchers D. Germain trusts endorse each paper. Same corpus, a different order for every researcher.
- α-Galactosidase A deficiency. Fabry disease
- New equations to estimate GFR in children with CKD. (Journal of the American Society of Nephrology)
- Enzyme replacement therapy in Fabry disease: a randomized controlled trial. (Journal of the American Medical Association (JAMA))
- Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males (Journal of Medical Genetics)
- Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females (Journal of Medical Genetics)
- Fabry Disease, an Under-Recognized Multisystemic Disorder: Expert Recommendations for Diagnosis, Management, and Enzyme Replacement Therapy (Annals of Internal Medicine)
- Long-Term Effects of Enzyme Replacement Therapy on Fabry Cardiomyopathy: Evidence for a Better Outcome With Early Treatment
- Elevated globotriaosylsphingosine is a hallmark of Fabry disease (Proceedings of the National Academy of Sciences of the United States of America)
- High incidence of later-onset fabry disease revealed by newborn screening. (American Journal of Human Genetics)
- [Fabry disease]. (Anais Brasileiros de Dermatologia)
Their papers
- Fabry disease (2010) — 617 citations
- Fabry Disease, an Under-Recognized Multisystemic Disorder: Expert Recommendations for Diagnosis, Management, and Enzyme Replacement Therapy (2003) — 747 citations