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Authors: Moldavsky, M Lev, D Lerman-Sagie, T
Citation: M. Moldavsky et al., Behavioral phenotypes of genetic syndromes: A reference guide for psychiatrists, J AM A CHIL, 40(7), 2001, pp. 749-761

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: Levine, A Watemberg, N Hager, H Bujanover, Y Ballin, A Lerman-Sagie, T
Citation: A. Levine et al., Benign intracranial hypertension associated with budesonide treatment in children with Crohn's disease, J CHILD NEU, 16(6), 2001, pp. 458-461

Authors: Lev, D Watemberg, N Aviram, A Fishoff, J Antman, E Lerman-Sagie, T
Citation: D. Lev et al., Febrile convulsions, ataxia, developmental delay, and obesity: A new syndrome?, J CHILD NEU, 16(3), 2001, pp. 174-176

Authors: Malinger, G Ginath, S Lerman-Sagie, T Watemberg, N Lev, D Glezerman, M
Citation: G. Malinger et al., The fetal cerebellar vermis: normal development as shown by transvaginal ultrasound, PRENAT DIAG, 21(8), 2001, pp. 687-692

Authors: Lerman-Sagie, T Rustin, P Lev, D Yanoov, M Leshinsky-Silver, E Sagie, A Ben-Gal, T Munnich, A
Citation: T. Lerman-sagie et al., Dramatic improvement in mitochondrial cardiomyopathy following treatment with idebenone, J INH MET D, 24(1), 2001, pp. 28-34

Authors: Nissenkorn, A Michelson, M Ben-Zeev, B Lerman-Sagie, T
Citation: A. Nissenkorn et al., Inborn errors of metabolism - A cause of abnormal brain development, NEUROLOGY, 56(10), 2001, pp. 1265-1272

Authors: Lerman-Sagie, T Watemberg, N Kramer, U Shahar, E Lerman, P
Citation: T. Lerman-sagie et al., Absence seizures aggravated by valproic acid, EPILEPSIA, 42(7), 2001, pp. 941-943

Authors: Wallace, RH Scheffer, IE Barnett, S Richards, M Dibbens, L Desai, RR Lerman-Sagie, T Lev, D Mazarib, A Brand, N Ben-Zeev, B Goikhman, I Singh, R Kremmidiotis, G Gardner, A Sutherland, GR George, AL Mulley, JC Berkovic, SF
Citation: Rh. Wallace et al., Neuronal sodium-channel alpha 1-subunit mutations in generalized epilepsy with febrile seizures plus, AM J HU GEN, 68(4), 2001, pp. 859-865

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: Haftel, LT Lev, D Barash, V Gutman, A Bujanover, Y Lerman-Sagie, T
Citation: Lt. Haftel et al., Familial mitochondrial intestinal pseudo-obstruction and neurogenic bladder, J CHILD NEU, 15(6), 2000, pp. 386-389

Authors: Watemberg, N Amsel, S Sadeh, M Lerman-Sagie, T
Citation: N. Watemberg et al., Common peroneal neuropathy due to surfing, J CHILD NEU, 15(6), 2000, pp. 420-421

Authors: Watemberg, N Leshner, RL Armstrong, BA Lerman-Sagie, T
Citation: N. Watemberg et al., Acute pediatric rhabdomyolysis, J CHILD NEU, 15(4), 2000, pp. 222-227

Authors: Nissenkorn, A Zeharia, A Lev, D Watemberg, N Fattal-Valevski, A Barash, V Gutman, A Harel, S Lerman-Sagie, T
Citation: A. Nissenkorn et al., Neurologic presentations of mitochondrial disorders, J CHILD NEU, 15(1), 2000, pp. 44-48

Authors: Malinger, G Lerman-Sagie, T Achiron, R Lipitz, S
Citation: G. Malinger et al., The subarachnoid space: normal fetal development as demonstrated by transvaginal ultrasound, PRENAT DIAG, 20(11), 2000, pp. 890-893

Authors: Lev, D Yanoov, M Weintraub, S Lerman-Sagie, T
Citation: D. Lev et al., Progressive neurological deterioration in a child with distal arthrogryposis and whistling face, J MED GENET, 37(3), 2000, pp. 231-233

Authors: Lorberboym, M Nissenkorn, A Avrahami, E Lerman-Sagie, T
Citation: M. Lorberboym et al., Technetium-99m-ethyl cysteinate dimer brain perfusion loss in pediatric postictal psychosis, SEM NUC MED, 30(3), 2000, pp. 234-236

Authors: Lerman-Sagie, T Houri, S Haftel, L Elpeleg, ON
Citation: T. Lerman-sagie et al., Mitochondrial DNA mutations are where to look, J CHILD NEU, 14(7), 1999, pp. 479-479

Authors: Zeharia, A Shuper, A Mimouni, M Kornreich, L Rachmel, A Lerman-Sagie, T
Citation: A. Zeharia et al., Periventricular brain heterotopias in a child with adrenocortical insufficiency, achalasia, alacrima, and neurologic abnormalities (Allgrove syndrome), J CHILD NEU, 14(5), 1999, pp. 331-334

Authors: Nissenkorn, A Moldavsky, M Lorberboym, M Raucher, A Bujanover, Y Lerman-Sagie, T
Citation: A. Nissenkorn et al., Postictal psychosis in a child, J CHILD NEU, 14(12), 1999, pp. 818-819

Authors: Lerman-Sagie, T Lerman, P
Citation: T. Lerman-sagie et P. Lerman, Phenobarbital still has a role in epilepsy treatment, J CHILD NEU, 14(12), 1999, pp. 820-821

Authors: Tanner, SM Orstavik, KH Kristiansen, M Lev, D Lerman-Sagie, T Sadeh, M Liechti-Gallati, S
Citation: Sm. Tanner et al., Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier mother, HUM GENET, 104(3), 1999, pp. 249-253

Authors: Azuri, J Lerman-Sagie, T Mizrahi, A Bujanover, Y
Citation: J. Azuri et al., Guillain-Barre syndrome following serological evidence of hepatitis A in achild, EUR J PED, 158(4), 1999, pp. 341-342

Authors: Azuri, J Mizrachi, A Weintraub, S Lerman-Sagie, T
Citation: J. Azuri et al., Neurological involvement in a child with the wrinkly skin syndrome, AM J MED G, 82(1), 1999, pp. 31-33

Authors: Michelson, M Harel, S Gutman, A Lerman-Sagie, T
Citation: M. Michelson et al., Urinary organic acid screening in children with developmental language delay, J INH MET D, 22(7), 1999, pp. 815-820
Risultati: 1-25 | 26-28