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Medical Journal (Fort Sam Houston, Tex.)|March 5, 2021
Installation Management Command's COVID-19 Pandemic Efforts Rely on Multiple Collaborative PartnershipsWilliam Paul Barras, Amelia M Duran-StantonClinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1975
Tyrosinemia and tyrosyluria in healthy prematures: time courses not vitamin C-dependentH D Bakker, S K Wadman, F J Van Sprang, et al.The Journal of Pediatrics|June 1, 1985
Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndromeP F Bougnères, F Rocchiccioli, S Kølvraa, et al.The Journal of Clinical Investigation|January 1, 1990
Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypesF Endo, A Tanoue, A Kitano, et al.Padiatrie Und Padologie|January 1, 1993
Diagnosis of mitochondrial fatty acid oxidation defectsM Duran, L Bruinvis, D Ketting, et al.Translational Research : the Journal of Laboratory and Clinical Medicine|August 14, 2012
The need for standardized protocols for future clinical trials of cell therapyJason M Duran, Sharven Taghavi, Jon C GeorgeArchives Francaises De Pediatrie|April 1, 1977
[The early diagnosis of Maroteaux-Lamy syndrome with confirmation of arylsulphatase deficiency]J P Van Biervliet, E F Van Leeuwen, N G Abeling, et al.Maturitas|October 1, 1992
Skin collagen changes related to age and hormone replacement therapyC Castelo-Branco, M Duran, J González-MerloMinerva Medica|October 1, 2011
Spontaneous rupture of fetal hydronephrosis: case reportA Kosus, N Kosus, M Duran, et al.Journal of Inherited Metabolic Disease|January 1, 1996
Congenital non-progressive encephalopathy and deafness with intermittent episodes of coma and hyperkynureninuriaR Cheminal, B Echenne, H Bellet, et al.Pageof 56