P173 – 2561: The clinical profile of ADHD in Israel – Impact of ethnic and social diversities
Mahajnah, M, Sharkia, R, Shorbaji, N, Terkel-Dawer, R, Zelnik, N
Published in European journal of paediatric neurology (01.05.2015)
Published in European journal of paediatric neurology (01.05.2015)
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Journal Article
A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab–Israeli family
Abu-Rashid, M, Mahajnah, M, Jaber, L, Kornreich, L, Bar-On, E, Basel-Vanagaite, L, Soffer, D, Koenig, M, Straussberg, R
Published in European journal of paediatric neurology (01.05.2013)
Published in European journal of paediatric neurology (01.05.2013)
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Journal Article
Cognition, psychosocial adjustment and coping in familial cases of velocardiofacial syndrome
Gothelf, D, Aviram-Goldring, A, Burg, M, Steinberg, T, Mahajnah, M, Frisch, A, Fennig, S, Zalsman, G, Weizman, A
Published in Journal of Neural Transmission (01.11.2007)
Published in Journal of Neural Transmission (01.11.2007)
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Journal Article
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures
Straussberg, R, Basel-Vanagaite, L, Kivity, S, Dabby, R, Cirak, S, Nurnberg, P, Voit, T, Mahajnah, M, Inbar, D, Saifi, G M, Lupski, J R, Delague, V, Megarbane, A, Richter, A, Leshinsky, E, Berkovic, S F
Published in Neurology (11.01.2005)
Published in Neurology (11.01.2005)
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Journal Article
A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an ArabaIsraeli family
Abu-Rashid, M, Mahajnah, M, Jaber, L, Kornreich, L, Bar-On, E, Basel-Vanagaite, L, Soffer, D, Koenig, M, Straussberg, R
Published in European journal of paediatric neurology (01.05.2013)
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Published in European journal of paediatric neurology (01.05.2013)
Journal Article
ASSOCIATION OF PARIETO-OCCIPITAL POLYMICROGYRIA, CHIARI MALFORMATION TYPE 1 AND SYRINGOMYELIA
Mahajnah, M, Lev Lev, D, Blumkin, L, Watemberg, N, Lerman-Sagie, T
Published in Neuropediatrics (18.05.2006)
Published in Neuropediatrics (18.05.2006)
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Conference Proceeding
Familial cognitive impairment with ataxia with oculomotor apraxia
Mahajnah, Muhammad, Basel-Vanagaite, Lina, Inbar, Dov, Kornreich, Liora, Weitz, Raphael, Straussberg, Rachel
Published in Journal of child neurology (01.06.2005)
Published in Journal of child neurology (01.06.2005)
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Journal Article
A Prospective Case Study of the Safety and Efficacy of Lysine-Restricted Diet and Arginine Supplementation Therapy in a Patient With Pyridoxine-Dependent Epilepsy Caused by Mutations in ALDH7A1
Mahajnah, Muhammad, MD, PhD, Corderio, Dawn, RN, Austin, Valerie, RD, Herd, Sarah, RD, Mutch, Carly, OT, Carter, Melissa, MD, Struys, Eduard, PhD, Mercimek-Mahmutoglu, Saadet, MD, PhD
Published in Pediatric neurology (01.07.2016)
Published in Pediatric neurology (01.07.2016)
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Journal Article