A novel mutation of late-onset very-long-chain acyl-CoA dehydrogenase deficiencySTRAUSSBERG, Rachel; STRAUSS, Arnold W.Pediatric neurology. 2002, Vol 27, Num 2, pp 136-137, issn 0887-8994Article

Pseudotumor cerebri manifesting as stiff neck and torticollisSTRAUSSBERG, Rachel; HAREL, Liora; AMIR, Jacob et al.Pediatric neurology. 2002, Vol 26, Num 3, pp 225-227, issn 0887-8994Article

Familial benign neonatal sleep myoclonusCOHEN, Rony; SHUPER, Avinoam; STRAUSSBERG, Rachel et al.Pediatric neurology. 2007, Vol 36, Num 5, pp 334-337, issn 0887-8994, 4 p.Article

Influence of circumcision technique on frequency of urinary tract infections in neonatesHAREL, Liora; STRAUSSBERG, Rachel; JACKSON, Shlomo et al.The Pediatric infectious disease journal. 2002, Vol 21, Num 9, pp 879-880, issn 0891-3668Article

Acute Cerebellitis Presenting as Tonsillar Herniation and HydrocephalusSHKALIM, Vered; AMIR, Jacob; KORNREICH, Liora et al.Pediatric neurology. 2009, Vol 41, Num 3, pp 200-203, issn 0887-8994, 4 p.Article

In vitro effect of statins on cytokine production and mitogen response of human peripheral blood mononuclear cellsBESSLER, Hanna; SALMAN, Hertzel; BERGMAN, Michael et al.Clinical immunology (Orlando, Fla. Print). 2005, Vol 117, Num 1, pp 73-77, issn 1521-6616, 5 p.Article

Pro- and anti-inflammatory cytokines in children with febrile convulsionsSTRAUSSBERG, Rachel; AMIR, Jacob; HAREL, Liora et al.Pediatric neurology. 2001, Vol 24, Num 1, pp 49-53, issn 0887-8994Article

Successful treatment of rheumatic chorea with carbamazepineHAREL, Liora; ZECHARIA, Abraham; STRAUSSBERG, Rachel et al.Pediatric neurology. 2000, Vol 23, Num 2, pp 147-151, issn 0887-8994Article

Acute motor axonal neuropathy-an atypical presentationLANDAU, Yuval E; DABBY, Ron; AMIR, Jacob et al.Pediatric neurology. 2007, Vol 36, Num 4, pp 271-273, issn 0887-8994, 3 p.Article

Treatment of calcinosis in juvenile dermatomyositis with probenecid : The role of phosphorus metabolism in the development of calcificationsHAREL, Liora; HAREL, Gideon; KORENREICH, Liora et al.Journal of rheumatology. 2001, Vol 28, Num 5, pp 1129-1132, issn 0315-162XConference Paper

Improvement of atypical acute disseminated encephalomyelitis with steroids and intravenous immunoglobulinsSTRAUSSBERG, Rachel; SCHONFELD, Tommy; WEITZ, Raphael et al.Pediatric neurology. 2001, Vol 24, Num 2, pp 139-143, issn 0887-8994Article

In vitro cytokine production in patients with iron deficiency anemiaBERGMAN, Michael; BESSLER, Hanna; SALMAN, Hertzel et al.Clinical immunology (Orlando, Fla. Print). 2004, Vol 113, Num 3, pp 340-344, issn 1521-6616, 5 p.Article

Phagocytic capacity and apoptosis of peripheral blood cells from patients with iron deficiency anemiaBERGMAN, Michael; SALMAN, Hertzel; PINCHASI, Rafael et al.Biomedicine & pharmacotherapy. 2005, Vol 59, Num 6, pp 307-311, issn 0753-3322, 5 p.Article

CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathyNEVO, Yoram; BEN-ZEEV, Bruria; ZENVIRT, Shamir et al.Blood. 2013, Vol 121, Num 1, pp 129-135, issn 0006-4971, 7 p.Article

Does a SCNIA gene mutation confer earlier age of onset of febrile seizures in GEFS+?SIJBEN, Angelique E. J; SITHINAMSUWAN, Pasiri; SCHEFFER, Ingrid E et al.Epilepsia (Copenhagen). 2009, Vol 50, Num 4, pp 953-956, issn 0013-9580, 4 p.Article

Microcephaly-Thin Corpus Callosum Syndrome Maps to 8q23.2-q24.12HALEVY, Ayelet; BASEL-VANAGAITE, Lina; NÜRNBERG, Peter et al.Pediatric neurology. 2012, Vol 46, Num 6, pp 363-368, issn 0887-8994, 6 p.Article

Infantile Cerebral and Cerebellar Atrophy Is Associated with a Mutation in the MED17 Subunit of the Transcription Preinitiation Mediator ComplexKAUFMANN, Rami; STRAUSSBERG, Rachel; DOBYNS, William B et al.American journal of human genetics. 2010, Vol 87, Num 5, pp 667-670, issn 0002-9297, 4 p.Article

A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia SyndromeBASSUK, Alexander G; WALLACE, Robyn H; SHU WU et al.American journal of human genetics. 2008, Vol 83, Num 5, pp 572-581, issn 0002-9297, 10 p.Article

A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal MicrocephalyMOCHIDA, Ganeshwaran H; MAHAJNAH, Muhammad; HILL, Anthony D et al.American journal of human genetics. 2009, Vol 85, Num 6, pp 897-902, issn 0002-9297, 6 p.Article

Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosisBASEL-VANAGAITE, Lina; MUNCHER, Liora; SHALEV, Hanna et al.Annals of neurology. 2006, Vol 60, Num 2, pp 214-222, issn 0364-5134, 9 p.Article

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21XIANHUA PIAO; BASEL-VANAGAITE, Lina; STRAUSSBERG, Rachel et al.American journal of human genetics. 2002, Vol 70, Num 4, pp 1028-1033, issn 0002-9297Article

X-linked Mental Retardation With Alacrima and Achalasia—Triple A Syndrome or A New Syndrome?MAROM, Daphna; ALBIN, Adi; SCHWARTZ, Charles et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 8, pp 1959-1963, issn 1552-4825, 5 p.Article

Thiamine deficiency in infants : MR findings in the brainKORNREICH, Liora; BRON-HARLEV, Efrat; HOREV, Gadi et al.American journal of neuroradiology. 2005, Vol 26, Num 7, pp 1668-1674, issn 0195-6108, 7 p.Article

Bilateral frontoparietal polymicrogyria: Clinical and radiological features in 10 families with linkage to chromosome 16CHANG, Bernard S; XIANHUA PIAO; GRANT, P. Ellen et al.Annals of neurology. 2003, Vol 53, Num 5, pp 596-606, issn 0364-5134, 11 p.Article