קהילה רפואית

מחקר בנושא נוירופדיאטריה

היחידה בשני בתי החולים מאבחנת ומטפלת בילדים עם דיסטרופיה שרירית, אפילפסיה, הפרעות בהתפתחות ומחלות נוירולוגיות אחרות. 

 

המרכז מספק שירות הכולל ביופסיות שריר ואלקטרופיזיולוגיה, אבחונים לליקויי למידה ועוד. 

 

לחצו על שם המחקר כדי לקבלו בצורת קובץ פי.די.אף PDF:

2005

Institutional Developmental Program in Muscular Dystrophies - Stiching Porticus

 

2006

CINRG International Grant - The role of aritifibrotic agents in ameliorating fibrosis in the dy and mdx mouse

 

2008-2009

Association Francaise contre Ia myopathie – "Evaluation of the therapeutic effect of Lorastan an angiotensin II type 1 antagonist as a novel therapy for congenital muscular dystrophy"

 

2008

CINRG International Grant - In vitro model for pre-screening of therapeutic agents in muscular dystrophy

 

2008-2009

Losartari - new treatment for muscular dystrophy. Ministry of health and Keren Ezvonot

 

2008

Horowitz - scientific industry collaboration grant - Glatiramer Acetate (GA) - Copaxone - a new treatment for muscular dystrophy

 

2009-2011

ISF - Israel Science Foundation - Combination of anti-inflammatory and anti-fibrotic therapy in muscular dystrophy

 

Electromyography (EMG) Accuracy Compared to Muscle Biopsy in Childhood, by: Malcolm Rabie, Joseph Jossiphov and Yoram Nevo, J Child Neurol 2007; 22; 803

 

Congenital Myopathies in Israeli Families, by: Karin Weiss, MD, Yehuda Shapira, MD, Benjamin Glick, MD, Tally Lerman-Sagie, MD, Eli Shahar, MD, Helly Goez, MD, Miriam Kutai, MD, and Yoram Nevo, MD, Journal of Child Neurology, Volume XX Number X, Month XXXX xx-xx

 

CINRG Randomized Controlled Trial of Creatine and Glutamine in Duchenne Muscular Dystrophy, by: Diana M. Escolar, MD, Gunnar Buyse, MD, PhD, Erik Henricson, MPH, Robert Leshner, MD, Julaine Florence, PT, DPT, Jill Mayhew, PT, Carolina Tesi-Rocha, MD, Ksenija Gorni, MD, Livia Pasquali, MD, Kantilal M. Patel, PhD, Robert McCarter, ScD, Jennifer Huang, PhD, MPH, Thomas Mayhew, PT, PhD, Tulio Bertorini, MD, Jose Carlo, MD, Anne M. Connolly, MD, Paula R. Clemens, MD, Nathalie Goemans, MD, Susan T. Iannaccone, MD, Masanori Igarashi, MD, Yoram Nevo, MD, Alan Pestronk, MD, S. H. Subramony, MD, V. V. Vedanarayanan, MD, Henry Wessel, MD, and the CINRG Goup, Ann Neurol 2005;58:151–155

 

Childhood acute and chronic immune-mediated polyradiculoneuropathies, by: Malcolm Rabie*, Yoram Nevo, European Journal of Paediatric Neurology xxx (2008) 1–10

 

Childhood chronic inflammatory demyelinating polyneuropathy, by: Yoram Nevo, European Journal of Paediatric Neurology 1998; 2: 169-177

 

88th ENMC International Workshop: Childhood chronic inflammatory demyelinating polyneuropathy (including revised diagnostic criteria), Naarden, The Netherlands, December 8–10, 2000, by: Yoram Nevo, Haluk Topaloglu, Neuromuscular Disorders 12 (2002) 195–200

 

Novel Mutations in the Emerin Gene in Israeli Families, by: Yoram Nevo, Sarit Ahituv, Yuval Yaron, Merav Kedmi, Ruth Shomrat, Cyril Legum, and Avi Orr-Urtreger, HUMAN MUTATION Mutation in Brief #422 (2001) Online

 

Fetal Muscle Biopsy as a Diagnostic Tool in Duchenne Muscular Dystrophy, by: Yoram Nevo, Ruth Shomrat, Yuval Yaron, Avi Orr-Urtreger, Shaul Harel AND Cyril Legum, PRENATAL DIAGNOSIS, 19: 921-926 (1999)

 

Childhood macrophagic myofasciitis—consanguinity and clinicopathological features, by: Yoram Nevo, Miriam Kutai, Joseph Jossiphov, Amir Livne, Zvi Neeman, Talmon Arad, Ronit Popovitz-Biro, Jacob Atsmon, Yehuda Shapira, Dov Soffer, Neuromuscular Disorders 14 (2004) 246–252

 

Clinical Characteristics and Muscle Pathology in Myopathic Mitochondrial DNA Depletion, by: Yoram Nevo, MD; Dov Soffer, MD; Miriam Kutai, MD; Nathanel Zelnik, MD; Anne Saada, PhD; Joseph Jossiphov, MD; Glenda Messer, PhD; Avraham Shagg, MSc; Eli Shahar, MD; Shaul Harel, MD; Orly Elpeleg, MD, Journal of Child Neurology / Volume 17, noumber 7, July 2002, pp. 499-504