Hurvitz H - Search Results

1

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. Hurvitz H, et al. Eur J Pediatr. 1989 Oct;149(1):48-51. doi: 10.1007/BF02024334. Eur J Pediatr. 1989. PMID: 2606128

2

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

Elpeleg ON, Christensen E, Hurvitz H, Branski D. Elpeleg ON, et al. Among authors: hurvitz h. Eur J Pediatr. 1990 Jul;149(10):709-12. doi: 10.1007/BF01959528. Eur J Pediatr. 1990. PMID: 2120061

3

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

Hurvitz H, Kerem E, Elpeleg ON, Barash V, Klar A, Mor C, Branski D. Hurvitz H, et al. Prog Clin Biol Res. 1989;306:143-8. Prog Clin Biol Res. 1989. PMID: 2740408 No abstract available.

4

Impaired kinetic properties of hypoxanthine-guanine phosphoribosyl transferase as a cause of uric acid nephropathy in early infancy.

Kerem E, Branski D, Gross-Kieselstein E, Hurvitz H, Abrahamov A, Pollack Y. Kerem E, et al. Among authors: hurvitz h. Eur J Pediatr. 1987 Nov;146(6):595-7. doi: 10.1007/BF02467362. Eur J Pediatr. 1987. PMID: 3428293

5

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

Elpeleg ON, Colombo JP, Amir N, Bachmann C, Hurvitz H. Elpeleg ON, et al. Among authors: hurvitz h. Eur J Pediatr. 1990 Jun;149(9):634-6. doi: 10.1007/BF02034751. Eur J Pediatr. 1990. PMID: 2373115

6

Hepatomegaly in utero in type III glycogenosis.

Reifen RM, Nadjari M, Hurvitz H, Barash V, Gutman A. Reifen RM, et al. Among authors: hurvitz h. Acta Paediatr Scand. 1989 Nov;78(6):954-5. doi: 10.1111/j.1651-2227.1989.tb11182.x. Acta Paediatr Scand. 1989. PMID: 2690567 No abstract available.

7

Chronic pigmented purpura: a case report of Schamberg's disease.

Kerem E, Branski D, Gross-Kieselstein E, Hurvitz H, Abrahamov A. Kerem E, et al. Among authors: hurvitz h. Clin Pediatr (Phila). 1987 Dec;26(12):657-8. doi: 10.1177/000992288702601209. Clin Pediatr (Phila). 1987. PMID: 3677535

8

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. Klar A, et al. Among authors: hurvitz h. Eur J Pediatr. 2010 Jun;169(6):727-32. doi: 10.1007/s00431-009-1102-1. Epub 2009 Nov 24. Eur J Pediatr. 2010. PMID: 19937054

9

Hallucinations and hyperthermia after promethazine ingestion.

Dollberg S, Hurvitz H, Kerem E, Navon P, Branski D. Dollberg S, et al. Among authors: hurvitz h. Acta Paediatr Scand. 1989 Jan;78(1):131-2. doi: 10.1111/j.1651-2227.1989.tb10902.x. Acta Paediatr Scand. 1989. PMID: 2919514 No abstract available.

10

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. Klar A, et al. Among authors: hurvitz h. J Pediatr. 1996 Jun;128(6):850-3. doi: 10.1016/s0022-3476(96)70340-2. J Pediatr. 1996. PMID: 8648547

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