Search details
1.
Evaluating platelet function disorders in children with bleeding tendency - A single center study.
Platelets
; 28(7): 676-681, 2017 Nov.
Article
in English
| MEDLINE | ID: mdl-28060550
2.
TMEM70 deficiency: long-term outcome of 48 patients.
J Inherit Metab Dis
; 38(3): 417-26, 2015 May.
Article
in English
| MEDLINE | ID: mdl-25326274
3.
Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder.
Pediatr Diabetes
; 15(3): 252-6, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24138066
4.
Establishing hospital admission criteria of pediatric Henoch-Schonlein purpura.
Rheumatol Int
; 34(11): 1497-503, 2014 Nov.
Article
in English
| MEDLINE | ID: mdl-24563020
5.
Extreme clinical variability of dilated cardiomyopathy in two siblings with Alström syndrome.
Pediatr Cardiol
; 34(2): 455-8, 2013 Feb.
Article
in English
| MEDLINE | ID: mdl-22447358
6.
TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome.
J Med Genet
; 48(3): 177-82, 2011 Mar.
Article
in English
| MEDLINE | ID: mdl-21147908
7.
SLC25A19 mutation as a cause of neuropathy and bilateral striatal necrosis.
Ann Neurol
; 66(3): 419-24, 2009 Sep.
Article
in English
| MEDLINE | ID: mdl-19798730
8.
Erratum to: TMEM70 deficiency: long-term outcome of 48 patients.
J Inherit Metab Dis
; 38(3): 583-4, 2015 May.
Article
in English
| MEDLINE | ID: mdl-25778942
9.
Age-related immunoglobulin G seroprevalence of human parvovirus B-19 in Israeli children.
Isr Med Assoc J
; 12(5): 277-9, 2010 May.
Article
in English
| MEDLINE | ID: mdl-20929079
10.
A new autosomal recessive syndrome characterized by ocular hypertelorism, distinctive face, mental retardation, brachydactyly, and genital abnormalities.
Am J Med Genet A
; 149A(12): 2655-60, 2009 Dec.
Article
in English
| MEDLINE | ID: mdl-19938075
11.
Pylephlebitis due to perforated appendicitis in a teenager.
Eur J Pediatr
; 168(5): 633-5, 2009 May.
Article
in English
| MEDLINE | ID: mdl-18762978
12.
Late relapse of herpes simplex virus encephalitis in a child due to reactivation of latent virus: clinicopathological report and review.
J Child Neurol
; 23(3): 344-8, 2008 Mar.
Article
in English
| MEDLINE | ID: mdl-18230840
13.
Diagnosis of familial Mediterranean fever following the initial presentation of monoarthritis.
Int J Rheum Dis
; 21(3): 755-760, 2018 Mar.
Article
in English
| MEDLINE | ID: mdl-27310037
14.
Acute human parvovirus B-19 infection in hospitalized children: A serologic and molecular survey.
Pediatr Infect Dis J
; 25(10): 898-901, 2006 Oct.
Article
in English
| MEDLINE | ID: mdl-17006284
15.
Secondary diabetes mellitus: late complication of glycogen storage disease type 1b.
J Pediatr Endocrinol Metab
; 18(6): 617-9, 2005 Jun.
Article
in English
| MEDLINE | ID: mdl-16042332
16.
Hospital admission trends for pediatric asthma: results of a 10 year survey in Israel.
Isr Med Assoc J
; 7(12): 785-9, 2005 Dec.
Article
in English
| MEDLINE | ID: mdl-16382700
17.
Acute neonatal suppurative parotitis: case reports and review.
Pediatr Infect Dis J
; 23(1): 76-8, 2004 Jan.
Article
in English
| MEDLINE | ID: mdl-14743054
18.
Clinico-pathological manifestations of variant late infantile neuronal ceroid lipofuscinosis (vLINCL) caused by a novel mutation in MFSD8 gene.
Eur J Med Genet
; 57(11-12): 607-12, 2014.
Article
in English
| MEDLINE | ID: mdl-25270050
19.
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy.
Eur J Hum Genet
; 22(7): 902-6, 2014 Jul.
Article
in English
| MEDLINE | ID: mdl-24281368
20.
Severe meningoencephalitis due to late reactivation of Varicella-Zoster virus in an immunocompetent child.
J Child Neurol
; 25(1): 87-90, 2010 Jan.
Article
in English
| MEDLINE | ID: mdl-19494359