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Results: 1-16 |
Results: 16

Authors: LEV D LERMANSAGIE T TANNER MS LIECHETIGALLATI S SADEH M
Citation: D. Lev et al., X-LINKED MYOTUBULAR MYOPATHY IN A WOMAN SUFFERING FROM PROGRESSIVE MUSCLE WEAKNESS, European journal of human genetics, 6, 1998, pp. 1068-1068

Authors: LERMANSAGIE T LERMAN P
Citation: T. Lermansagie et P. Lerman, DRAMATIC EFFECT OF LAMOTRIGINE IN YOUNG-ADULTS SUFFERING FROM INTRACTABLE ABSENCES AND GENERALIZED TONIC-CLONIC SEIZURES SINCE CHILDHOOD, Journal of epilepsy, 11(3), 1998, pp. 148-151

Authors: NISSENKORN A WEINTRAUB S SADEH M LERMANSAGIE T
Citation: A. Nissenkorn et al., LISSENCEPHALY ASSOCIATED WITH CONGENITAL HYPOMYELINATING AND AXONAL NEUROPATHY, Pediatric neurology, 19(4), 1998, pp. 313-316

Authors: LERMANSAGIE T MESHULACH I GUTMAN A
Citation: T. Lermansagie et al., TRANSIENT PRIMARY CARNITINE DEFICIENCY, Journal of inherited metabolic disease, 21(4), 1998, pp. 425-426

Authors: LERMANSAGIE T BERNS L TOMER A GLICK B ARIEL I HAREL S
Citation: T. Lermansagie et al., CENTRAL-NERVOUS-SYSTEM INVOLVEMENT IN X-LINKED MYOTUBULAR MYOPATHY, Journal of child neurology, 12(1), 1997, pp. 70-73

Authors: PARVARI R LEI KJ BASHAN N HERSHKOVITZ E KORMAN SH BARASH V LERMANSAGIE T MANDEL H CHOU JY MOSES SW
Citation: R. Parvari et al., GLYCOGEN-STORAGE-DISEASE TYPE 1A IN ISRAEL - BIOCHEMICAL, CLINICAL, AND MUTATIONAL STUDIES, American journal of medical genetics, 72(3), 1997, pp. 286-290

Authors: MOLDAVSKY M LERMANSAGIE T KUTAI M LEGUM C HAREL S
Citation: M. Moldavsky et al., HETEROGENEITY IN ADDUCTED THUMBS SEQUENCE, American journal of medical genetics, 70(2), 1997, pp. 114-117

Authors: HANSEN A GUERINA N LERMANSAGIE T KORSON M
Citation: A. Hansen et al., CENTRAL APNEA IN A CHILD WITH CONGENITAL AUTONOMIC DYSFUNCTION AND UNIVERSAL PAIN LOSS, Journal of child neurology, 11(2), 1996, pp. 162-164

Authors: LERMANSAGIE T FILIANO J SMITH DW KORSON M
Citation: T. Lermansagie et al., INFANTILE ONSET OF HEREDITARY ASCENDING SPASTIC PARALYSIS WITH BULBARINVOLVEMENT, Journal of child neurology, 11(1), 1996, pp. 54-57

Authors: LERMANSAGIE T
Citation: T. Lermansagie, BEHR SYNDROME, Pediatric neurology, 12(1), 1995, pp. 90-90

Authors: LERMAN P LERMANSAGIE T
Citation: P. Lerman et T. Lermansagie, SULTHIAME REVISITED, Journal of child neurology, 10(3), 1995, pp. 241-242

Authors: LERMAN P LERMANSAGIE T
Citation: P. Lerman et T. Lermansagie, LOW-DOSE PHENOBARBITAL MONOTHERAPY IN PRIMARY EPILEPSY - LONG-TERM FOLLOW-UP-STUDY, Epilepsia, 36, 1995, pp. 265-266

Authors: LERMANSAGIE T MIMOUNI M
Citation: T. Lermansagie et M. Mimouni, REVERSAL OF ANOREXIA IN A CHILD WITH PARTIAL ORNITHINE TRANSCARBAMYLASE DEFICIENCY BY CYPROHEPTADINE THERAPY, Clinical pediatrics, 34(3), 1995, pp. 163-165

Authors: GARTY BZ OLOMUCKI R LERMANSAGIE T NITZAN M
Citation: Bz. Garty et al., CEREBROSPINAL-FLUID ZINC CONCENTRATIONS IN FEBRILE CONVULSIONS, Archives of Disease in Childhood, 73(4), 1995, pp. 338-341

Authors: BONNEMANN CG LERMANSAGIE T KOSOFSKY BE ROBINSON BH SOTREL A DOUGHERTY FE SIMS KB
Citation: Cg. Bonnemann et al., LEIGH-DISEASE DUE TO COMPLEX-I DEFICIENCY PRESENTING AS LEUKODYSTROPHY, Annals of neurology, 36(3), 1994, pp. 543-543

Authors: LERMANSAGIE T LERMAN P MUKAMEL M BLIEDEN L MIMOUNI M
Citation: T. Lermansagie et al., A PROSPECTIVE EVALUATION OF PEDIATRIC-PATIENTS WITH SYNCOPE, Clinical pediatrics, 33(2), 1994, pp. 66-70
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