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Journal of Inherited Metabolic Disease|September 10, 2005
Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentationM A Cleary, L Dorland, T J de Koning, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|March 23, 2022
Cryptococcal Meningitis Reported With Fingolimod Treatment: Case SeriesMaurizio Del Poeta, Brian J Ward, Benjamin Greenberg, et al.
Science (New York, N.Y.)|September 10, 2011
Australopithecus sediba at 1.977 Ma and implications for the origins of the genus HomoRobyn Pickering, Paul H G M Dirks, Zubair Jinnah, et al.
Ophthalmic Research|November 11, 2016
Identifying Predictors of Anti-VEGF Treatment Response in Patients with Neovascular Age-Related Macular Degeneration through Discriminant and Principal Component AnalysisFrank G Holz, Ramin Tadayoni, Stephen Beatty, et al.
Circulation|August 1, 1981
Angiographic prevalence of high-risk coronary artery disease in patient subsets (CASS)B R Chaitman, M G Bourassa, K Davis, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|May 9, 2015
Documented atrial fibrillation recurrences after pulmonary vein isolation are associated with diminished quality of lifeWouter R Berger, Sébastien P J Krul, Joy A van der Pol, et al.
Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|January 24, 2026
Lesion characteristics after pulsed-field ablation in patients with paroxysmal atrial fibrillation and a left common ostium (PFALCO RE-MAP STUDY)Daniel Mol, Erik A Stel, Wouter R Berger, et al.
Journal of Hepatology|October 30, 2001
FIC1, the protein affected in two forms of hereditary cholestasis, is localized in the cholangiocyte and the canalicular membrane of the hepatocyteE F Eppens, S W van Mil, J M de Vree, et al.
Neurology|January 29, 2003
Oxidative stress in HIV demented patients and protection ex vivo with novel antioxidantsJ Turchan, C B Pocernich, C Gairola, et al.
Genomics|April 1, 1991
Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22P J Willems, J Hendrickx, B J Van der Auwera, et al.
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