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Items: 1 to 50 of 64

1.

Two novel mutations identified in familial cases with Donohue syndrome.

Falik Zaccai TC, Kalfon L, Klar A, Elisha MB, Hurvitz H, Weingarten G, Chechik E, Fleisher Sheffer V, Haj Yahya R, Meidan G, Gross-Kieselstein E, Bauman D, Hershkovitz S, Yaron Y, Orr-Urtreger A, Wertheimer E.

Mol Genet Genomic Med. 2014 Jan;2(1):64-72. doi: 10.1002/mgg3.43. Epub 2013 Nov 14.

2.

Cellular and clinical report of new Griscelli syndrome type III cases.

Westbroek W, Klar A, Cullinane AR, Ziegler SG, Hurvitz H, Ganem A, Wilson K, Dorward H, Huizing M, Tamimi H, Vainshtein I, Berkun Y, Lavie M, Gahl WA, Anikster Y.

Pigment Cell Melanoma Res. 2012 Jan;25(1):47-56. doi: 10.1111/j.1755-148X.2011.00901.x. Epub 2011 Oct 3.

3.

Prolidase deficiency: it looks like systemic lupus erythematosus but it is not.

Klar A, Navon-Elkan P, Rubinow A, Branski D, Hurvitz H, Christensen E, Khayat M, Falik-Zaccai TC.

Eur J Pediatr. 2010 Jun;169(6):727-32. doi: 10.1007/s00431-009-1102-1. Epub 2009 Nov 24.

PMID:
19937054
4.

Atrial natriuretic Peptide in young and elderly children with mild gastroenteritis.

Klar A, Haver E, Lichtstein D, Hurvitz H, Foah-Shauli T.

Gastroenterol Res Pract. 2009;2009:623871. doi: 10.1155/2009/623871. Epub 2009 Jul 1.

5.

Acute otitis media in the first two months of life: characteristics and diagnostic difficulties.

Berkun Y, Nir-Paz R, Ami AB, Klar A, Deutsch E, Hurvitz H.

Arch Dis Child. 2008 Aug;93(8):690-4. doi: 10.1136/adc.2007.127522. Epub 2008 Mar 12.

PMID:
18337275
6.

Three novel mutations in POU1F1 in Israeli patients with combined pituitary hormone deficiency.

Gat-Yablonski G, Klar A, Hirsch D, Eliakim A, Lazar L, Hurvitz H, Phillip M.

J Pediatr Endocrinol Metab. 2005 Apr;18(4):385-93.

PMID:
15844473
7.

Atrial natriuretic peptide in children with pneumonia.

Haviv M, Haver E, Lichtstein D, Hurvitz H, Klar A.

Pediatr Pulmonol. 2005 Oct;40(4):306-9.

PMID:
15830390
8.

Sludge ball, pseudolithiasis, cholelithiasis and choledocholithiasis from intrauterine life to 2 years: a 13-year follow-up.

Klar A, Branski D, Akerman Y, Nadjari M, Berkun Y, Moise J, Shazberg G, Revel-Vilk S, Israeli T, Katz G, Levy A, Ami AB, Hurvitz H.

J Pediatr Gastroenterol Nutr. 2005 Apr;40(4):477-80.

PMID:
15795598
9.

Kingella kingae endocarditis and sepsis in an infant.

Berkun Y, Brand A, Klar A, Halperin E, Hurvitz H.

Eur J Pediatr. 2004 Nov;163(11):687-8. Epub 2004 Aug 6. No abstract available.

PMID:
15300433
10.

Rasmussen encephalitis with active inflammation and delayed seizures onset.

Korn-Lubetzki I, Bien CG, Bauer J, Gomori M, Wiendl H, Trajo L, Ovadia H, Wilken B, Hans VH, Elger CE, Hurvitz H, Steiner I.

Neurology. 2004 Mar 23;62(6):984-6.

PMID:
15037707
11.

Intestinal protein loss and hypoalbuminemia in children with pneumonia.

Klar A, Shoseyov D, Berkun Y, Brand A, Braun J, Shazberg G, Jonathan M, Gross-Kieselstein E, Revel-Vilk S, Hurvitz H.

J Pediatr Gastroenterol Nutr. 2003 Aug;37(2):120-3.

PMID:
12883295
12.

Early peripheral nervous system manifestations of infantile Krabbe disease.

Korn-Lubetzki I, Dor-Wollman T, Soffer D, Raas-Rothschild A, Hurvitz H, Nevo Y.

Pediatr Neurol. 2003 Feb;28(2):115-8.

PMID:
12699861
13.

Involvement of human heparanase in the pathogenesis of diabetic nephropathy.

Katz A, Van-Dijk DJ, Aingorn H, Erman A, Davies M, Darmon D, Hurvitz H, Vlodavsky I.

Isr Med Assoc J. 2002 Nov;4(11):996-1002.

14.

Chronic human parvovirus B19 infection associated with interstitial lung disease.

Klar A, Halamish A, Shoseyov D, Cassinotti P, Siegl G, Springer C, Shazberg G, Hurvitz H.

Isr Med Assoc J. 2002 Oct;4(10):825-6. No abstract available.

15.

Transmission of the mitochondrial t8993c mutation in a new family.

Hurvitz H, Naveh Y, Shoseyov D, Klar A, Shaag A, Elpeleg O.

Am J Med Genet. 2002 Sep 1;111(4):446-7. No abstract available.

PMID:
12210309
16.

Evidence that Griscelli syndrome with neurological involvement is caused by mutations in RAB27A, not MYO5A.

Anikster Y, Huizing M, Anderson PD, Fitzpatrick DL, Klar A, Gross-Kieselstein E, Berkun Y, Shazberg G, Gahl WA, Hurvitz H.

Am J Hum Genet. 2002 Aug;71(2):407-14. Epub 2002 Jun 7. Erratum in: Am J Hum Genet 2002 Oct;71(4):1007.

17.

Salmonella mastitis in a child.

Klar A, Shazberg G, Levichek Z, Halamish A, Hurvitz H.

Clin Pediatr (Phila). 2002 Apr;41(3):201. No abstract available.

PMID:
11999687
18.

Short-term course and outcome of treatments of pleural empyema in pediatric patients: repeated ultrasound-guided needle thoracocentesis vs chest tube drainage.

Shoseyov D, Bibi H, Shatzberg G, Klar A, Akerman J, Hurvitz H, Maayan C.

Chest. 2002 Mar;121(3):836-40.

PMID:
11888969
19.

Mutation analysis of the FAH gene in Israeli patients with tyrosinemia type I.

Elpeleg ON, Shaag A, Holme E, Zughayar G, Ronen S, Fisher D, Hurvitz H.

Hum Mutat. 2002 Jan;19(1):80-1.

PMID:
11754109
20.

MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.

Schenk B, Imbach T, Frank CG, Grubenmann CE, Raymond GV, Hurvitz H, Korn-Lubetzki I, Revel-Vik S, Raas-Rotschild A, Luder AS, Jaeken J, Berger EG, Matthijs G, Hennet T, Aebi M.

J Clin Invest. 2001 Dec;108(11):1687-95. Erratum in: J Clin Invest. 2003 Mar;111(6):925.

21.

Corticosteroid therapy reversed progressive chronic granulomatous lung disease following deterioration on interferon-gamma treatment.

Halamish A, Klar A, Shoseyov D, Blinder G, Hurvitz H.

Pediatr Pulmonol. 2001 Sep;32(3):257-60.

PMID:
11536456
22.

The clinical course of bronchiolitis associated with acute otitis media.

Shazberg G, Revel-Vilk S, Shoseyov D, Ben-Ami A, Klar A, Hurvitz H.

Arch Dis Child. 2000 Oct;83(4):317-9.

23.

Hepatitis A associated with other focal infections.

Klar A, Gross-Kieselstein E, Shazberg G, Israeli T, Revel-Vilk S, Hurvitz H.

Isr Med Assoc J. 2000 Aug;2(8):598-600.

24.

Perforated gastric ulcer complicating corticosteroid therapy in acute rheumatic fever.

Klar A, Moise J, Brand A, Seror D, Hurvitz H.

Acta Gastroenterol Belg. 2000 Apr-Jun;63(2):236-8.

PMID:
10925477
25.

Recurrent acute disseminated encephalomyelitis associated with acute cytomegalovirus and Epstein-Barr virus infection.

Revel-Vilk S, Hurvitz H, Klar A, Virozov Y, Korn-Lubetzki I.

J Child Neurol. 2000 Jun;15(6):421-4.

PMID:
10868789
26.

Muscular carnitine palmitoyltransferase II deficiency in infancy.

Hurvitz H, Klar A, Korn-Lubetzki I, Wanders RJ, Elpeleg ON.

Pediatr Neurol. 2000 Feb;22(2):148-50.

PMID:
10738923
27.

Family outbreak of Rickettsia conorii infection.

Shazberg G, Moise J, Terespolsky N, Hurvitz H.

Emerg Infect Dis. 1999 Sep-Oct;5(5):723-4. No abstract available.

28.

Gallbladder and pancreatic involvement in hepatitis A.

Klar A, Branski D, Nadjari M, Akerman MY, Shoseyov D, Hurvitz H.

J Clin Gastroenterol. 1998 Sep;27(2):143-5.

PMID:
9754776
29.

Treatment with hypertonic saline versus normal saline nasal wash of pediatric chronic sinusitis.

Shoseyov D, Bibi H, Shai P, Shoseyov N, Shazberg G, Hurvitz H.

J Allergy Clin Immunol. 1998 May;101(5):602-5.

PMID:
9600495
30.

Focal bacterial nephritis (lobar nephronia) in children.

Klar A, Hurvitz H, Berkun Y, Nadjari M, Blinder G, Israeli T, Halamish A, Katz A, Shazberg G, Branski D.

J Pediatr. 1996 Jun;128(6):850-3.

PMID:
8648547
31.

Functional endoscopic sinus surgery of orbital subperiosteal abscess in children.

Deutsch E, Eilon A, Hevron I, Hurvitz H, Blinder G.

Int J Pediatr Otorhinolaryngol. 1996 Jan;34(1-2):181-90.

PMID:
8770688
32.

Lipomatosis of the scalp and macrocephaly.

Lusthaus SN, Benmeir P, Ashur H, Neuman A, Weinberg A, Hurvitz H, Klar A, Gross-Kieselstein I, Wexler MR.

Plast Reconstr Surg. 1995 Jan;95(1):130-2.

PMID:
7809225
33.

A kindred with Griscelli disease: spectrum of neurological involvement.

Hurvitz H, Gillis R, Klaus S, Klar A, Gross-Kieselstein F, Okon E.

Eur J Pediatr. 1993 May;152(5):402-5.

PMID:
8319705
34.

Deteriorating neurological and neuroradiological course in treated biotinidase deficiency.

Ginat-Israeli T, Hurvitz H, Klar A, Blinder G, Branski D, Amir N.

Neuropediatrics. 1993 Apr;24(2):103-6.

PMID:
8327062
35.

Cardiomyopathy in lipodystrophy and the specificity spillover hypothesis.

Klar A, Brand A, Hurvitz H, Gross-Kieselstein E, Branski D.

Isr J Med Sci. 1993 Jan;29(1):50-2. No abstract available.

PMID:
8454451
36.

Haemophilus influenzae type b purpura fulminans treated with hyperbaric oxygen.

Dollberg S, Nachum Z, Klar A, Engelhard D, Ginat-Israeli T, Hurvitz H, Melamed Y, Branski D.

J Infect. 1992 Sep;25(2):197-200.

PMID:
1431173
37.

Eicosanoids content in small intestinal mucosa of children with celiac disease.

Branski D, Hurvitz H, Halevi A, Klar A, Navon P, Weidenfeld J.

J Pediatr Gastroenterol Nutr. 1992 Feb;14(2):173-6.

PMID:
1317423
38.

Barrett's esophagus in a young patient with Raynaud's phenomenon.

Navon P, Klar A, Hurvitz H, Adler SN, Branski D.

J Rheumatol. 1991 Nov;18(11):1735-6.

PMID:
1787496
39.

Recurrent, familial Reye-like syndrome with a new complex amino and organic aciduria.

Elpeleg ON, Christensen E, Hurvitz H, Branski D.

Eur J Pediatr. 1990 Jul;149(10):709-12.

PMID:
2120061
40.

Late-onset form of partial N-acetylglutamate synthetase deficiency.

Elpeleg ON, Colombo JP, Amir N, Bachmann C, Hurvitz H.

Eur J Pediatr. 1990 Jun;149(9):634-6.

PMID:
2373115
41.

Succinic acidemia is not a new syndrome of organic acidemia.

Elpeleg ON, Hurvitz H.

Clin Chim Acta. 1990 May;188(3):271-2. No abstract available.

PMID:
2387080
42.

Seizures in the course of hepatitis A.

Dollberg S, Hurvitz H, Reifen RM, Navon P, Branski D.

Am J Dis Child. 1990 Feb;144(2):140-1. No abstract available.

PMID:
2301314
43.

Hepatomegaly in utero in type III glycogenosis.

Reifen RM, Nadjari M, Hurvitz H, Barash V, Gutman A.

Acta Paediatr Scand. 1989 Nov;78(6):954-5. No abstract available.

PMID:
2690567
44.

Glycogen storage disease, Fanconi nephropathy, abnormal galactose metabolism and mitochondrial myopathy.

Hurvitz H, Elpeleg ON, Barash V, Kerem E, Reifen RM, Ruitenbeek W, Mor C, Branski D.

Eur J Pediatr. 1989 Oct;149(1):48-51.

PMID:
2606128
45.

Biotinidase deficiency associated with severe combined immunodeficiency.

Hurvitz H, Ginat-Israeli T, Elpeleg ON, Klar A, Amir N.

Lancet. 1989 Jul 22;2(8656):228-9. No abstract available.

PMID:
2568564
46.

Fructose-1,6-diphosphatase deficiency: a 20-year follow-up.

Elpeleg ON, Barash V, Hurvitz H, Branski D.

Am J Dis Child. 1989 Feb;143(2):140-2. No abstract available. Erratum in: Am J Dis Child 1989 Nov;143(11):1345.

PMID:
2916480
47.

Hallucinations and hyperthermia after promethazine ingestion.

Dollberg S, Hurvitz H, Kerem E, Navon P, Branski D.

Acta Paediatr Scand. 1989 Jan;78(1):131-2. No abstract available.

PMID:
2919514
48.

Mitochondrial myopathy, Fanconi syndrome with impaired glycogen and galactose metabolism.

Hurvitz H, Kerem E, Elpeleg ON, Barash V, Klar A, Mor C, Branski D.

Prog Clin Biol Res. 1989;306:143-8. No abstract available.

PMID:
2740408
49.

[Results of screening for organic aciduria in Israel].

Elpeleg O, Amir N, Hurvitz H, Navon P, Christensen E.

Harefuah. 1988 Dec 15;115(12):377-9. Hebrew. No abstract available.

PMID:
3240901
50.

Group D streptococcal neonatal mastitis.

Dollberg S, Hurvitz H, Klar A, Engelhard D.

Pediatr Infect Dis J. 1988 May;7(5):362. No abstract available.

PMID:
3132696

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