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Inflammatory Bowel Diseases|August 15, 2015
Abnormal Liver Biochemistry Is Common in Pediatric Inflammatory Bowel Disease: Prevalence and AssociationsPamela L Valentino, Brian M Feldman, Thomas D Walters, et al.
Biochimica Et Biophysica Acta|June 15, 2007
Biochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993Alessandra Baracca, Gianluca Sgarbi, Marina Mattiazzi, et al.
European Journal of Medical Genetics|September 12, 2015
A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathyL Licchetta, F Bisulli, M Fietz, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 28, 2001
Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two casesV Carelli, M L Valentino, R Liguori, et al.
Pediatric Transplantation|May 4, 2024
Optimizing pediatric liver transplantation: Evaluating the impact of donor age and graft type on patient survival outcomeYong K Kwon, Pamela L Valentino, Patrick J Healey, et al.
Neurology|September 15, 2006
Infusion of platelets transiently reduces nucleoside overload in MNGIEM C Lara, B Weiss, I Illa, et al.
Peptides|September 1, 1988
Pancreastatin distribution and plasma levels in the pigD Bretherton-Watt, M A Ghatei, A E Bishop, et al.
Italian Journal of Neurological Sciences|December 31, 1997
Searching for migraine genes: exclusion of 290 cM out of the whole human genomeL Monari, M Mochi, M L Valentino, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|July 9, 2013
The role of diagnostic imaging and liver biopsy in the diagnosis of focal nodular hyperplasia in childrenPamela L Valentino, Simon C Ling, Vicky L Ng, et al.
The Journal of Molecular Diagnostics : JMD|July 27, 2007
Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approachAnna Genasetti, Maria L Valentino, Valerio Carelli, et al.
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