Korman SH - Search Results

1

Methylenetetrahydrofolate reductase deficiency: importance of early diagnosis.

Fattal-Valevski A, Bassan H, Korman SH, Lerman-Sagie T, Gutman A, Harel S. Fattal-Valevski A, et al. Among authors: korman sh. J Child Neurol. 2000 Aug;15(8):539-43. doi: 10.1177/088307380001500808. J Child Neurol. 2000. PMID: 10961793

2

Estimation of glucose carbon recycling in children with glycogen storage disease: A 13C NMR study using [U-13C]glucose.

Kalderon B, Korman SH, Gutman A, Lapidot A. Kalderon B, et al. Among authors: korman sh. Proc Natl Acad Sci U S A. 1989 Jun;86(12):4690-4. doi: 10.1073/pnas.86.12.4690. Proc Natl Acad Sci U S A. 1989. PMID: 2734314 Free PMC article.

3

Glucose recycling and production in glycogenosis type I and III: stable isotope technique study.

Kalderon B, Korman SH, Gutman A, Lapidot A. Kalderon B, et al. Among authors: korman sh. Am J Physiol. 1989 Sep;257(3 Pt 1):E346-53. doi: 10.1152/ajpendo.1989.257.3.E346. Am J Physiol. 1989. PMID: 2782400

4

Glucose recycling and production in children with glycogen storage disease type I, studied by gas chromatography/mass spectrometry and (U-13C)glucose.

Kalderon B, Lapidot A, Korman SH, Gutman A. Kalderon B, et al. Among authors: korman sh. Biomed Environ Mass Spectrom. 1988 Oct;16(1-12):305-8. doi: 10.1002/bms.1200160158. Biomed Environ Mass Spectrom. 1988. PMID: 3242682

5

Muscle carnitine deficiency presenting as familial fatal cardiomyopathy.

Colin AA, Jaffe M, Shapira Y, Ne'eman Z, Gutman A, Korman S. Colin AA, et al. Arch Dis Child. 1987 Nov;62(11):1170-2. doi: 10.1136/adc.62.11.1170. Arch Dis Child. 1987. PMID: 3688923 Free PMC article.

6

Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studies.

Parvari R, Lei KJ, Bashan N, Hershkovitz E, Korman SH, Barash V, Lerman-Sagie T, Mandel H, Chou JY, Moses SW. Parvari R, et al. Among authors: korman sh. Am J Med Genet. 1997 Oct 31;72(3):286-90. doi: 10.1002/(sici)1096-8628(19971031)72:3<286::aid-ajmg6>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9332655

7

Characteristic urine organic acid profile in peroxisomal biogenesis disorders.

Korman SH, Mandel H, Gutman A. Korman SH, et al. J Inherit Metab Dis. 2000 Jun;23(4):425-8. doi: 10.1023/a:1005624523611. J Inherit Metab Dis. 2000. PMID: 10896310 No abstract available.

8

Carnitine-deficient myopathy as a presentation of tyrosinemia type I.

Nissenkorn A, Korman SH, Vardi O, Levine A, Katzir Z, Ballin A, Lerman-Sagie T. Nissenkorn A, et al. Among authors: korman sh. J Child Neurol. 2001 Sep;16(9):642-4. doi: 10.1177/088307380101600903. J Child Neurol. 2001. PMID: 11575602

9

Phenotype and genotype variation in primary carnitine deficiency.

Wang Y, Korman SH, Ye J, Gargus JJ, Gutman A, Taroni F, Garavaglia B, Longo N. Wang Y, et al. Among authors: korman sh. Genet Med. 2001 Nov-Dec;3(6):387-92. doi: 10.1097/00125817-200111000-00002. Genet Med. 2001. PMID: 11715001 Free article.

10

A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.

Raas-Rothschild A, Wanders RJ, Mooijer PA, Gootjes J, Waterham HR, Gutman A, Suzuki Y, Shimozawa N, Kondo N, Eshel G, Espeel M, Roels F, Korman SH. Raas-Rothschild A, et al. Among authors: korman sh. Am J Hum Genet. 2002 Apr;70(4):1062-8. doi: 10.1086/339766. Epub 2002 Feb 28. Am J Hum Genet. 2002. PMID: 11873320 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

104 results

Search Page

Filters