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Results: 1-25 | 26-28
Results: 1-25/28
Simultaneous recording of late and ultra-late pain evoked potentials in fibromyalgia
Authors: Granot, M Buskila, D Granovsky, Y Sprecher, E Neumann, L Yarnitsky, D
Citation: M. Granot et al., Simultaneous recording of late and ultra-late pain evoked potentials in fibromyalgia, CLIN NEU, 112(10), 2001, pp. 1881-1887
Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin
Authors: Sprecher, E Bergman, R Richard, G Lurie, R Shalev, S Petronius, D Shalata, A Anbinder, Y Leibu, R Perlman, I Cohen, N Szargel, R
Citation: E. Sprecher et al., Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin, NAT GENET, 29(2), 2001, pp. 134-136
Consolidation radiation therapy following cytoreductive surgery, chemotherapy and second-look laparotomy for epithelial ovarian carcinoma: Long-term follow-up
Authors: Goldberg, H Stein, ME Steiner, M Sprecher, E Beck, D Kuten, A
Citation: H. Goldberg et al., Consolidation radiation therapy following cytoreductive surgery, chemotherapy and second-look laparotomy for epithelial ovarian carcinoma: Long-term follow-up, TUMORI, 87(4), 2001, pp. 248-251
Immunogenetics of HLA class II in Israeli Ashkenazi Jewish, Israeli non-Ashkenazi Jewish, and in Israeli Arab IDDM patients
Authors: Kwon, OJ Brautbar, C Weintrob, N Sprecher, E Saphirman, C Bloch, K Pinhas-Hamiel, O Assah, S Vardi, P Israel, S
Citation: Oj. Kwon et al., Immunogenetics of HLA class II in Israeli Ashkenazi Jewish, Israeli non-Ashkenazi Jewish, and in Israeli Arab IDDM patients, HUMAN IMMUN, 62(1), 2001, pp. 85-91
Type I diabetes environmental factors and correspondence analysis of HLA class II genes in the Yemenite Jewish community in Israel
Authors: Weintrob, N Sprecher, E Israel, S Pinhas-Hamiel, O Kwon, OJ Bloch, K Abramov, N Arbel, A Josefsberg, Z Brautbar, C Vardi, P
Citation: N. Weintrob et al., Type I diabetes environmental factors and correspondence analysis of HLA class II genes in the Yemenite Jewish community in Israel, DIABET CARE, 24(4), 2001, pp. 650-653
The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: Implications for mutation detection and first case of prenataldiagnosis
Authors: Sprecher, E Chavanas, S DiGiovanna, JJ Amin, S Nielsen, K Prendiville, JS Silverman, R Esterly, NB Spraker, MK Guelig, E de Luna, ML Williams, ML Buehler, B Siegfried, EC Van Maldergem, L Pfendner, E Bale, SJ Uitto, J Hovnanian, A Richard, G
Citation: E. Sprecher et al., The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: Implications for mutation detection and first case of prenataldiagnosis, J INVES DER, 117(2), 2001, pp. 179-187
Evidence for novel functions of the keratin tail emerging from a mutation causing ichthyosis hystrix
Authors: Sprecher, E Ishida-Yamamoto, A Becker, OM Marekov, L Miller, CJ Steinert, PM Nelder, K Richard, G
Citation: E. Sprecher et al., Evidence for novel functions of the keratin tail emerging from a mutation causing ichthyosis hystrix, J INVES DER, 116(4), 2001, pp. 511-519
Diabetes and ischemic heart disease among Yemenite immigrants in Israel
Authors: Weingarten, MA Katzir, I Sprecher, E Kobzantsev, S Zelzer, C Kahan, E
Citation: Ma. Weingarten et al., Diabetes and ischemic heart disease among Yemenite immigrants in Israel, ISR MED ASS, 2(3), 2000, pp. 207-210
Combined clonidine-short-ACTH test for the simultaneous assessment of growth hormone reserve and hypothalamic-pituitary-adrenal axis integrity in children
Authors: Weintrob, N Sprecher, E Josefsberg, Z Vardi, P Weininger, C Aurbach-Klipper, Y Pertzelan, A Phillip, M
Citation: N. Weintrob et al., Combined clonidine-short-ACTH test for the simultaneous assessment of growth hormone reserve and hypothalamic-pituitary-adrenal axis integrity in children, EUR J ENDOC, 143(1), 2000, pp. 105-110
Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
Authors: Sprecher, E Shalata, A Dabhah, K Futerman, B Lin, S Szargel, R Bergman, R Friedman-Birnbaum, R Cohen, N
Citation: E. Sprecher et al., Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene, J AM ACAD D, 42(6), 2000, pp. 978-982
A comparative immunohistochemical study of MART-1 expression in Spitz nevi, ordinary melanocytic nevi, and malignant melanomas
Authors: Bergman, R Azzam, H Sprecher, E Manov, L Munichor, M Friedman-Birnbaum, R Ben-Itzhak, O
Citation: R. Bergman et al., A comparative immunohistochemical study of MART-1 expression in Spitz nevi, ordinary melanocytic nevi, and malignant melanomas, J AM ACAD D, 42(3), 2000, pp. 496-500
Homogeneity of the age at diagnosis in sibs with type 2 diabetes: Implications for sib-pair analysis
Authors: Lev-Ran, A Sprecher, E Yerushalmy, Y Schindel, B Kisch, ES
Citation: A. Lev-ran et al., Homogeneity of the age at diagnosis in sibs with type 2 diabetes: Implications for sib-pair analysis, AM J MED G, 91(2), 2000, pp. 91-94
Normative values for female genital sensation
Authors: Vardi, Y Gruenwald, I Sprecher, E Gertman, I Yarnitsky, D
Citation: Y. Vardi et al., Normative values for female genital sensation, UROLOGY, 56(6), 2000, pp. 1035-1040
Diffuse alveolar hemorrhage following thrombolytic therapy for acute myocardial infarction
Authors: Yigla, M Sprecher, E Azzam, Z Guralnik, L Kapeliovich, M Krivoy, N
Citation: M. Yigla et al., Diffuse alveolar hemorrhage following thrombolytic therapy for acute myocardial infarction, RESPIRATION, 67(4), 2000, pp. 445-448
Logistic regression and survival analysis of 450 impotent patients treatedwith injection therapy: Long-term dropout parameters
Authors: Vardi, Y Sprecher, E Gruenwald, I
Citation: Y. Vardi et al., Logistic regression and survival analysis of 450 impotent patients treatedwith injection therapy: Long-term dropout parameters, J UROL, 163(2), 2000, pp. 467-470
Settling the score on hairless - Reply
Authors: Sprecher, E Lestringant, GG Szargel, R Bergman, R Labay, V Frossard, PM Friedman-Birnbaum, R Cohen, N
Citation: E. Sprecher et al., Settling the score on hairless - Reply, J INVES DER, 115(4), 2000, pp. 762-763
Netherton syndrome is not linked to 18q12, a region homologous to the murine Lanceolate Hair (lah) locus
Authors: Sprecher, E Bale, SJ DiGiovanna, JJ Uitto, J Richard, G
Citation: E. Sprecher et al., Netherton syndrome is not linked to 18q12, a region homologous to the murine Lanceolate Hair (lah) locus, J INVES DER, 114(4), 2000, pp. 741-742
Monitoring of the extracranial and intracranial course of single emboli ofcardiac origin: A preliminary report
Authors: Telman, G Reisner, SA Sprecher, E Hemli, JA Yarnitsky, D
Citation: G. Telman et al., Monitoring of the extracranial and intracranial course of single emboli ofcardiac origin: A preliminary report, J NEUROIMAG, 9(4), 1999, pp. 238-240
Cyclosporine treatment of psoriatic erythroderma complicated by bacterial sepsis
Authors: Sprecher, E Bergman, R Friedman-Birnbaum, R
Citation: E. Sprecher et al., Cyclosporine treatment of psoriatic erythroderma complicated by bacterial sepsis, J EUR A D V, 12(2), 1999, pp. 197-198
Apoptosis, Fas and Fas-ligand expression in melanocytic tumors
Authors: Sprecher, E Bergman, R Meilick, A Kerner, H Manov, L Reiter, I Shafer, Y Maor, G Friedman-Birnbaum, R
Citation: E. Sprecher et al., Apoptosis, Fas and Fas-ligand expression in melanocytic tumors, J CUT PATH, 26(2), 1999, pp. 72-77
Limitations of quantitative sensory testing when patients are biased toward a bad outcome
Authors: Yarnitsky, D Sprecher, E Zaslansky, R Baron, R Bowsher, D Boivie, J Casey, K Claus, D Hanson, P Lindblom, U Marchettini, P Parry, GJ Verdugo, R
Citation: D. Yarnitsky et al., Limitations of quantitative sensory testing when patients are biased toward a bad outcome, NEUROLOGY, 52(4), 1999, pp. 894-894
Atrichia with papular lesions resulting from a nonsense mutation within the human hairless gene
Authors: Sprecher, E Lestringant, GG Szargel, R Bergman, R Labay, V Frossard, PM Friedman-Birnbaum, R Cohen, N
Citation: E. Sprecher et al., Atrichia with papular lesions resulting from a nonsense mutation within the human hairless gene, J INVES DER, 113(4), 1999, pp. 687-690
Paradoxical heat sensation in healthy subjects: peripherally conducted by A delta or C fibres?
Authors: Susser, E Sprecher, E Yarnitsky, D
Citation: E. Susser et al., Paradoxical heat sensation in healthy subjects: peripherally conducted by A delta or C fibres?, BRAIN, 122, 1999, pp. 239-246
Identification of a genetic defect in the hairless gene in atrichia with papular lesions: Evidence for phenotypic heterogeneity among inherited atrichias
Authors: Sprecher, E Bergman, R Szargel, R Friedman-Birnbaum, R Cohen, N
Citation: E. Sprecher et al., Identification of a genetic defect in the hairless gene in atrichia with papular lesions: Evidence for phenotypic heterogeneity among inherited atrichias, AM J HU GEN, 64(5), 1999, pp. 1323-1329
Reduced folate carrier (RFC-1) gene expression in normal and psoriatic skin
Authors: Sprecher, E Bergman, R Sprecher, H Maor, G Reiter, I Krivoy, N Drori, S Assaraf, YG Friedman-Birnbaum, R
Citation: E. Sprecher et al., Reduced folate carrier (RFC-1) gene expression in normal and psoriatic skin, ARCH DERM R, 290(12), 1998, pp. 656-660
Risultati: 1-25 | 26-28