Lerman-Sagie T - Search Results

1

Familial mitochondrial intestinal pseudo-obstruction and neurogenic bladder.

Haftel LT, Lev D, Barash V, Gutman A, Bujanover Y, Lerman-Sagie T. Haftel LT, et al. J Child Neurol. 2000 Jun;15(6):386-9. doi: 10.1177/088307380001500606. J Child Neurol. 2000. PMID: 10868781

2

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. 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

3

Transient 'primary' carnitine deficiency.

Lerman-Sagie T, Meshulach I, Gutman A. Lerman-Sagie T, et al. J Inherit Metab Dis. 1998 Jun;21(4):425-6. doi: 10.1023/a:1005366927461. J Inherit Metab Dis. 1998. PMID: 9700601 No abstract available.

4

Guillain-Barre syndrome following serological evidence of hepatitis A in a child.

Azuri J, Lerman-Sagie T, Mizrahi A, Bujanover Y. Azuri J, et al. Eur J Pediatr. 1999 Apr;158(4):341-2. doi: 10.1007/s004310051086. Eur J Pediatr. 1999. PMID: 10206138 No abstract available.

5

Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier mother.

Tanner SM, Orstavik KH, Kristiansen M, Lev D, Lerman-Sagie T, Sadeh M, Liechti-Gallati S. Tanner SM, et al. Hum Genet. 1999 Mar;104(3):249-53. doi: 10.1007/s004390050943. Hum Genet. 1999. PMID: 10323249

6

Demyelinative brainstem encephalitis responsive to intravenous immunoglobulin therapy.

Assa A, Watemberg N, Bujanover Y, Lerman-Sagie T. Assa A, et al. Pediatrics. 1999 Aug;104(2 Pt 1):301-3. doi: 10.1542/peds.104.2.301. Pediatrics. 1999. PMID: 10429012

7

Multiple presentation of mitochondrial disorders.

Nissenkorn A, Zeharia A, Lev D, Fatal-Valevski A, Barash V, Gutman A, Harel S, Lerman-Sagie T. Nissenkorn A, et al. Arch Dis Child. 1999 Sep;81(3):209-14. doi: 10.1136/adc.81.3.209. Arch Dis Child. 1999. PMID: 10451392 Free PMC article.

8

Urinary organic acid screening in children with developmental language delay.

Michelson M, Harel S, Gutman A, Lerman-Sagie T. Michelson M, et al. J Inherit Metab Dis. 1999 Oct;22(7):815-20. doi: 10.1023/a:1005558108125. J Inherit Metab Dis. 1999. PMID: 10518282

9

Mitochondrial DNA mutations are where to look.

Lerman-Sagie T, Haftel L, Elpeleg ON. Lerman-Sagie T, et al. J Child Neurol. 1999 Jul;14(7):479. doi: 10.1177/088307389901400716. J Child Neurol. 1999. PMID: 10573475 No abstract available.

10

Postictal psychosis in a child.

Nissenkorn A, Moldavsky M, Lorberboym M, Raucher A, Bujanover Y, Lerman-Sagie T. Nissenkorn A, et al. J Child Neurol. 1999 Dec;14(12):818-9. doi: 10.1177/088307389901401209. J Child Neurol. 1999. PMID: 10614570

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