Joe McMenamin

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder

Willemijn G. Leen, Jörg Klepper, Marcel M. Verbeek et al. · Brain · 2010 · 413 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Mental retardation linked to mutations in the <i>HSD17B10</i> gene interfering with neurosteroid and isoleucine metabolism

Song‐Yu Yang, Xue‐Ying He, S. E. Olpin et al. · Proceedings of the National Academy of Sciences · 2009 · 50 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

2‐Methyl‐3‐hydroxybutyryl‐CoA dehydrogenase deficiency in a 23‐year‐old man

S. E. Olpin, R. J. Pollitt, Joe McMenamin et al. · Journal of Inherited Metabolic Disease · 2002 · 45 citations · Full text

Life Sciences, Biochemistry, Enzymology +7

Bannayan-Riley-Ruvalcaba syndrome: a cause of extreme macrocephaly and neurodevelopmental delay

Niamh E. Lynch, Sally Ann Lynch, Joe McMenamin et al. · Archives of Disease in Childhood · 2009 · 42 citations

Medicine, Genetics, Molecular Genetics +17

Aggravation of Seizures by Antiepileptic Drugs: What to Do in Clinical Practice

Pierre Genton, Joe McMenamin · Epilepsia · 1998 · 38 citations · Full text

Medicine, Neurology, Pharmacology +14