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Results: 1-25 |
Results: 25
ONCE VERSUS TWICE-DAILY INJECTIONS OF GROWTH-HORMONE IN CHILDREN WITHIDIOPATHIC SHORT STATURE
Authors: PHILLIP M HERSHKOVITZ E BELOTSERKOVSKY O LEIBERMAN E LIMONI Y ZADIK Z
Citation: M. Phillip et al., ONCE VERSUS TWICE-DAILY INJECTIONS OF GROWTH-HORMONE IN CHILDREN WITHIDIOPATHIC SHORT STATURE, Acta paediatrica, 87(5), 1998, pp. 518-520
INCREASE OF SERUM-LIPOPROTEIN (A) LEVELS DURING GROWTH-HORMONE THERAPY IN NORMAL SHORT CHILDREN
Authors: HERSHKOVITZ E BELOTSERKOVSKY O LIMONY Y LEIBERMAN E SHANY S PHILLIP M
Citation: E. Hershkovitz et al., INCREASE OF SERUM-LIPOPROTEIN (A) LEVELS DURING GROWTH-HORMONE THERAPY IN NORMAL SHORT CHILDREN, European journal of pediatrics, 157(1), 1998, pp. 4-7
SERUM INSULIN-LIKE GROWTH-FACTOR-I AND GROWTH-FACTOR-II ARE NOT AFFECTED BY UNDERNUTRITION IN CHILDREN WITH NONORGANIC FAILURE-TO-THRIVE
Authors: PHILLIP M HERSHKOVITZ E ROSENBLUM H SAVION I SEGEV Y LEVY J FRAZER D
Citation: M. Phillip et al., SERUM INSULIN-LIKE GROWTH-FACTOR-I AND GROWTH-FACTOR-II ARE NOT AFFECTED BY UNDERNUTRITION IN CHILDREN WITH NONORGANIC FAILURE-TO-THRIVE, Hormone research, 49(2), 1998, pp. 76-79
2 NEW MUTATIONS IN THE 3'-CODING REGION OF THE GLYCOGEN DEBRANCHING ENZYME IN A GLYCOGEN-STORAGE-DISEASE TYPE IIIA ASHKENAZI JEWISH PATIENT
Authors: PARVARI R SHEN J HERSHKOVITZ E CHEN YT MOSES SW
Citation: R. Parvari et al., 2 NEW MUTATIONS IN THE 3'-CODING REGION OF THE GLYCOGEN DEBRANCHING ENZYME IN A GLYCOGEN-STORAGE-DISEASE TYPE IIIA ASHKENAZI JEWISH PATIENT, Journal of inherited metabolic disease, 21(2), 1998, pp. 141-148
A 4TH-ORDER NUMERICAL INTEGRATOR FOR STOCHASTIC LANGEVIN-EQUATIONS
Authors: HERSHKOVITZ E
Citation: E. Hershkovitz, A 4TH-ORDER NUMERICAL INTEGRATOR FOR STOCHASTIC LANGEVIN-EQUATIONS, The Journal of chemical physics, 108(22), 1998, pp. 9253-9258
HOMOZYGOSITY AND LINKAGE-DISEQUILIBRIUM MAPPING OF THE SYNDROME OF CONGENITAL HYPOPARATHYROIDISM, GROWTH AND MENTAL-RETARDATION, AND DYSMORPHISM TO A 1-CM INTERVAL ON CHROMOSOME 1Q42-43
Authors: PARVARI R HERSHKOVITZ E KANIS A GORODISCHER R SHALITIN S SHEFFIELD VC CARMI R
Citation: R. Parvari et al., HOMOZYGOSITY AND LINKAGE-DISEQUILIBRIUM MAPPING OF THE SYNDROME OF CONGENITAL HYPOPARATHYROIDISM, GROWTH AND MENTAL-RETARDATION, AND DYSMORPHISM TO A 1-CM INTERVAL ON CHROMOSOME 1Q42-43, American journal of human genetics, 63(1), 1998, pp. 163-169
THE GENE FOR GLYCOGEN-STORAGE-DISEASE TYPE 1B MAPS TO CHROMOSOME 11Q23
Authors: ANNABI B HIRAIWA H MANSFIELD BC LEI KJ UBAGAI T POLYMEROPOULOS MH MOSES SW PARVARI R HERSHKOVITZ E MANDEL H FRYMAN M CHOU JY
Citation: B. Annabi et al., THE GENE FOR GLYCOGEN-STORAGE-DISEASE TYPE 1B MAPS TO CHROMOSOME 11Q23, American journal of human genetics, 62(2), 1998, pp. 400-405
A SINGLE-BASE DELETION IN THE 3'-CODING REGION OF GLYCOGEN-DEBRANCHING ENZYME IS PREVALENT IN GLYCOGEN-STORAGE-DISEASE TYPE IIIA IN A POPULATION OF NORTH-AFRICAN JEWISH PATIENTS
Authors: PARVARI R MOSES S SHEN JJ HERSHKOVITZ E LERNER A CHEN YT
Citation: R. Parvari et al., A SINGLE-BASE DELETION IN THE 3'-CODING REGION OF GLYCOGEN-DEBRANCHING ENZYME IS PREVALENT IN GLYCOGEN-STORAGE-DISEASE TYPE IIIA IN A POPULATION OF NORTH-AFRICAN JEWISH PATIENTS, European journal of human genetics, 5(5), 1997, pp. 266-270
SUBNORMAL CORTISOL RESPONSE TO ADRENOCORTICOTROPIN IN ISOLATED PARTIAL 17,20-LYASE DEFICIENCY
Authors: LEIBERMAN E HERSHKOVITZ E LAUBERBIASON A PHILLIP M ZACHMANN M
Citation: E. Leiberman et al., SUBNORMAL CORTISOL RESPONSE TO ADRENOCORTICOTROPIN IN ISOLATED PARTIAL 17,20-LYASE DEFICIENCY, Journal of pediatric endocrinology & metabolism, 10(4), 1997, pp. 387-390
GLYCOGEN-STORAGE-DISEASE TYPE 1A IN ISRAEL - BIOCHEMICAL, CLINICAL, AND MUTATIONAL STUDIES
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
MULTIDIMENSIONAL GENERALIZATION OF THE POLLAK-GRABERT-HANGGI TURNOVERTHEORY FOR ACTIVATED RATE-PROCESSES
Authors: HERSHKOVITZ E POLLAK E
Citation: E. Hershkovitz et E. Pollak, MULTIDIMENSIONAL GENERALIZATION OF THE POLLAK-GRABERT-HANGGI TURNOVERTHEORY FOR ACTIVATED RATE-PROCESSES, The Journal of chemical physics, 106(18), 1997, pp. 7678-7699
AN EARLY RISE IN URINE N-TELOPEPTIDE PREDICTS THE GROWTH-RESPONSE OF NORMAL PREPUBERTAL SHORT CHILDREN TO GROWTH-HORMONE THERAPY
Authors: PHILLIP M HERSHKOVITZ E LIMONI Y LEIBERMAN E BELOTSERKOVSKY O DOUVDEVANI A WEBER D
Citation: M. Phillip et al., AN EARLY RISE IN URINE N-TELOPEPTIDE PREDICTS THE GROWTH-RESPONSE OF NORMAL PREPUBERTAL SHORT CHILDREN TO GROWTH-HORMONE THERAPY, Journal of pediatric endocrinology & metabolism, 9(5), 1996, pp. 519-521
SHORT-TERM GROWTH-HORMONE THERAPY INCREASES SERUM-LIPOPROTEIN (A) LEVELS IN NORMAL SHORT CHILDREN WITHOUT GROWTH-HORMONE DEFICIENCY
Authors: HERSHKOVITZ E LEIBERMAN E LIMONY Y SHANY S PHILLIP M
Citation: E. Hershkovitz et al., SHORT-TERM GROWTH-HORMONE THERAPY INCREASES SERUM-LIPOPROTEIN (A) LEVELS IN NORMAL SHORT CHILDREN WITHOUT GROWTH-HORMONE DEFICIENCY, Hormone research, 46(1), 1996, pp. 38-40
PRENATAL-DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE 1A BY SINGLE-STRANDED CONFORMATION POLYMORPHISM (SSCP)
Authors: PARVARI R HERSHKOVITZ E CARMI R MOSES S
Citation: R. Parvari et al., PRENATAL-DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE 1A BY SINGLE-STRANDED CONFORMATION POLYMORPHISM (SSCP), Prenatal diagnosis, 16(9), 1996, pp. 862-865
PRENATAL-DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE 1A BY SSCP ANALYSIS
Authors: MOSES S HERSHKOVITZ E CARMI R PARVARI R
Citation: S. Moses et al., PRENATAL-DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE 1A BY SSCP ANALYSIS, Pediatric research, 39(4), 1996, pp. 868-868
STATUS EPILEPTICUS FOLLOWING INTRAVENOUS N-ACETYLCYSTEINE THERAPY
Authors: HERSHKOVITZ E SHORER Z LEVITAS A TAL A
Citation: E. Hershkovitz et al., STATUS EPILEPTICUS FOLLOWING INTRAVENOUS N-ACETYLCYSTEINE THERAPY, Israel journal of medical sciences, 32(11), 1996, pp. 1102-1104
ADRENAL INSUFFICIENCY AFTER ACHALASIA IN THE TRIPLE-A SYNDROME
Authors: PHILLIP M HERSHKOVITZ E SCHULMAN H
Citation: M. Phillip et al., ADRENAL INSUFFICIENCY AFTER ACHALASIA IN THE TRIPLE-A SYNDROME, Clinical pediatrics, 35(2), 1996, pp. 99-100
DIFFERENCES IN CORD SERUM RETINOL CONCENTRATIONS BY ETHNIC-ORIGIN IN THE NEGEV (SOUTHERN ISRAEL)
Authors: GORODISCHER R SAROV B GAZALA E HERSHKOVITZ E EDWARDSON S SKLAN D KATZ M
Citation: R. Gorodischer et al., DIFFERENCES IN CORD SERUM RETINOL CONCENTRATIONS BY ETHNIC-ORIGIN IN THE NEGEV (SOUTHERN ISRAEL), Early human development, 42(2), 1995, pp. 123-130
THYROTROPIN-SECRETING PITUITARY-ADENOMA ASSOCIATED WITH HYPOPITUITARISM AND DIABETES-INSIPIDUS IN AN ADOLESCENT BOY
Authors: PHILLIP M HERSHKOVITZ E KORNMEHL P COHEN A LEIBERMAN E
Citation: M. Phillip et al., THYROTROPIN-SECRETING PITUITARY-ADENOMA ASSOCIATED WITH HYPOPITUITARISM AND DIABETES-INSIPIDUS IN AN ADOLESCENT BOY, Journal of pediatric endocrinology & metabolism, 8(1), 1995, pp. 47-50
RFLPS FOR LINKAGE ANALYSIS IN FAMILIES WITH GLYCOGEN-STORAGE-DISEASE TYPE-III
Authors: MISHORIDERY A BASHAN N MOSES S HERSHKOVITZ E BAO Y CHEN YT PARVARI R
Citation: A. Mishoridery et al., RFLPS FOR LINKAGE ANALYSIS IN FAMILIES WITH GLYCOGEN-STORAGE-DISEASE TYPE-III, Journal of inherited metabolic disease, 18(2), 1995, pp. 207-210
CHARACTERIZATION OF THE MUTATIONS IN THE GLUCOSE-6-PHOSPHATASE GENE IN ISRAELI PATIENTS WITH GLYCOGEN-STORAGE-DISEASE TYPE-1A - R83C IN 6 JEWS AND A NOVEL V166G MUTATION IN A MUSLIM ARAB
Authors: PARVARI R MOSES S HERSHKOVITZ E CARMI R BASHAN N
Citation: R. Parvari et al., CHARACTERIZATION OF THE MUTATIONS IN THE GLUCOSE-6-PHOSPHATASE GENE IN ISRAELI PATIENTS WITH GLYCOGEN-STORAGE-DISEASE TYPE-1A - R83C IN 6 JEWS AND A NOVEL V166G MUTATION IN A MUSLIM ARAB, Journal of inherited metabolic disease, 18(1), 1995, pp. 21-27
HIGH PREVALENCE OF THYROXINE-BINDING GLOBULIN DEFICIENCY AMONG BEDOUIN INFANTS IN SOUTHERN ISRAEL
Authors: HERSHKOVITZ E LEIBERMAN E REFETOFF S PILPELL D PHILLIP M
Citation: E. Hershkovitz et al., HIGH PREVALENCE OF THYROXINE-BINDING GLOBULIN DEFICIENCY AMONG BEDOUIN INFANTS IN SOUTHERN ISRAEL, Israel journal of medical sciences, 31(8), 1995, pp. 500-502
THE NEW SYNDROME OF CONGENITAL HYPOPARATHYROIDISM ASSOCIATED WITH DYSMORPHISM, GROWTH-RETARDATION, AND DEVELOPMENTAL DELAY - A REPORT OF 6 PATIENTS
Authors: HERSHKOVITZ E SHALITIN S LEVY J LEIBERMAN E WEINSHTOCK A VARSANO I GORODISCHER R
Citation: E. Hershkovitz et al., THE NEW SYNDROME OF CONGENITAL HYPOPARATHYROIDISM ASSOCIATED WITH DYSMORPHISM, GROWTH-RETARDATION, AND DEVELOPMENTAL DELAY - A REPORT OF 6 PATIENTS, Israel journal of medical sciences, 31(5), 1995, pp. 293-297
PRENATAL ULTRASONIC DIAGNOSIS OF NONHYPERTROPHIC PYLORIC-STENOSIS ASSOCIATED WITH INTESTINAL MALROTATION
Authors: HERSHKOVITZ E STEINER Z SHINWELL ES MEIZNER I
Citation: E. Hershkovitz et al., PRENATAL ULTRASONIC DIAGNOSIS OF NONHYPERTROPHIC PYLORIC-STENOSIS ASSOCIATED WITH INTESTINAL MALROTATION, Journal of clinical ultrasound, 22(1), 1994, pp. 52-54
LUTEINIZING-HORMONE-RELEASING HORMONE ANTAGONISTS INTERFERE WITH AUTOCRINE AND PARACRINE GROWTH-STIMULATION OF MCF-7 MAMMARY-CANCER CELLS BY INSULIN-LIKE GROWTH-FACTORS
Authors: HERSHKOVITZ E MARBACH M BOSIN E LEVY J ROBERTS CT LEROITH D SCHALLY AV SHARONI Y
Citation: E. Hershkovitz et al., LUTEINIZING-HORMONE-RELEASING HORMONE ANTAGONISTS INTERFERE WITH AUTOCRINE AND PARACRINE GROWTH-STIMULATION OF MCF-7 MAMMARY-CANCER CELLS BY INSULIN-LIKE GROWTH-FACTORS, The Journal of clinical endocrinology and metabolism, 77(4), 1993, pp. 963-968
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