AAAAAA
Results:
1-7
|
Results: 7
Authors:
Wang, YH
Korman, SH
Ye, J
Gargus, JJ
Gutman, A
Taroni, F
Garavaglia, B
Longo, N
Citation: Yh. Wang et al., Phenotype and genotype variation in primary carnitine deficiency, GENET MED, 3(6), 2001, pp. 387-392
Authors:
Nissenkorn, A
Korman, SH
Vardi, O
Levine, A
Katzir, Z
Ballin, A
Lerman-Sagie, T
Citation: A. Nissenkorn et al., Carnitine-deficient myopathy as a presentation of tyrosinemia type I, J CHILD NEU, 16(9), 2001, pp. 642-644
Authors:
Elpeleg, ON
Korman, SH
Citation: On. Elpeleg et Sh. Korman, Sustained oral lysine supplementation in ornithine delta-aminotransferase deficiency, J INH MET D, 24(3), 2001, pp. 423-424
Authors:
Straussberg, R
Saiag, E
Harel, L
Korman, SH
Amir, J
Citation: R. Straussberg et al., Reversible deafness caused by biotinidase deficiency, PED NEUROL, 23(3), 2000, pp. 269-270
Authors:
Fattal-Valevski, A
Bassan, H
Korman, SH
Lerman-Sagie, T
Gutman, A
Harel, S
Citation: A. Fattal-valevski et al., Methylenetetrahydrofolate reductase deficiency: Importance of early diagnosis, J CHILD NEU, 15(8), 2000, pp. 539-543
Authors:
Levy-Khademi, F
Korman, SH
Amitai, Y
Citation: F. Levy-khademi et al., Henoch-Schonlein purpura: Simultaneous occurrence in two siblings, PEDIAT DERM, 17(2), 2000, pp. 139-140
Authors:
Korman, SH
Mandel, H
Gutman, A
Citation: Sh. Korman et al., Characteristic urine organic acid profile in peroxisomal biogenesis disorders, J INH MET D, 23(4), 2000, pp. 425-428
Risultati:
1-7
|