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E Pras

Showing results (81-90 of 100) with videos related to

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European Journal of Human Genetics : EJHG|April 21, 2001
A single mutated MEFV allele in Israeli patients suffering from familial Mediterranean fever and Behçet's disease (FMF-BD)A Livneh, I Aksentijevich, P Langevitz, et al.
Clinical Genetics|January 11, 2014
Founder mutation for Huntington disease in Caucasus JewsO Melamed, D M Behar, C Bram, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex)C A Stratakis, R B Jenkins, E Pras, et al.
American Journal of Human Genetics|November 13, 2001
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelH Lahat, E Pras, T Olender, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|July 1, 1996
Concurrent chemo- and radiotherapy in patients with locally advanced carcinoma of the cervixE Pras, P H Willemse, H Boonstra, et al.
Clinical Genetics|October 23, 2014
Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndromeD Oz-Levi, B Weiss, A Lahad, et al.
European Journal of Cancer (Oxford, England : 1990)|February 10, 2009
Long-term morbidity of adjuvant whole abdominal radiotherapy (WART) or chemotherapy for early stage ovarian cancerM J A Engelen, B J Snel, M Schaapveld, et al.
Anticancer Research|March 16, 2004
Paclitaxel and carboplatin concurrent with radiotherapy for primary cervical cancerF Y F L de Vos, A M E Bos, J A Gietema, et al.
The Journal of Rheumatology|August 1, 1997
Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: two diseases with distinct clinical, serologic, and genetic featuresA Livneh, J P Drenth, I S Klasen, et al.
American Journal of Human Genetics|March 26, 1999
Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish populationI Aksentijevich, Y Torosyan, J Samuels, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
European Journal of Human Genetics : EJHG|April 21, 2001
A single mutated MEFV allele in Israeli patients suffering from familial Mediterranean fever and Behçet's disease (FMF-BD)A Livneh, I Aksentijevich, P Langevitz, et al.
Clinical Genetics|January 11, 2014
Founder mutation for Huntington disease in Caucasus JewsO Melamed, D M Behar, C Bram, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex)C A Stratakis, R B Jenkins, E Pras, et al.
American Journal of Human Genetics|November 13, 2001
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelH Lahat, E Pras, T Olender, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|July 1, 1996
Concurrent chemo- and radiotherapy in patients with locally advanced carcinoma of the cervixE Pras, P H Willemse, H Boonstra, et al.
Clinical Genetics|October 23, 2014
Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndromeD Oz-Levi, B Weiss, A Lahad, et al.
European Journal of Cancer (Oxford, England : 1990)|February 10, 2009
Long-term morbidity of adjuvant whole abdominal radiotherapy (WART) or chemotherapy for early stage ovarian cancerM J A Engelen, B J Snel, M Schaapveld, et al.
Anticancer Research|March 16, 2004
Paclitaxel and carboplatin concurrent with radiotherapy for primary cervical cancerF Y F L de Vos, A M E Bos, J A Gietema, et al.
The Journal of Rheumatology|August 1, 1997
Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: two diseases with distinct clinical, serologic, and genetic featuresA Livneh, J P Drenth, I S Klasen, et al.
American Journal of Human Genetics|March 26, 1999
Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish populationI Aksentijevich, Y Torosyan, J Samuels, et al.
Pageof 10