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B Hamel

Showing results (91-100 of 103) with videos related to

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Annals of Internal Medicine|January 29, 2000
Resource use and survival of patients hospitalized with congestive heart failure: differences in care by specialty of the attending physician. SUPPORT Investigators. Study to Understand Prognoses and Preferences for Outcomes and Risks of TreatmentsA D Auerbach, M B Hamel, R B Davis, et al.
Journal of the American College of Cardiology|December 29, 2000
Patient characteristics associated with care by a cardiologist among adults hospitalized with severe congestive heart failure. SUPPORT Investigators. Study to Understand Prognoses and Preferences for Outcomes and Risks of TreatmentsA D Auerbach, M B Hamel, R M Califf, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlationsM R Nelen, H Kremer, I B Konings, et al.
Journal of Medical Genetics|November 25, 2003
A homozygous nonsense mutation in the fukutin gene causes a Walker-Warburg syndrome phenotypeD Beltrán-Valero de Bernabé, H van Bokhoven, E van Beusekom, et al.
American Journal of Medical Genetics|July 9, 1999
X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: the European XLMR consortiumV des Portes, C Beldjord, J Chelly, et al.
Circulation|August 26, 1998
Resuscitation preferences among patients with severe congestive heart failure: results from the SUPPORT project. Study to Understand Prognoses and Preferences for Outcomes and Risks of TreatmentsH M Krumholz, R S Phillips, M B Hamel, et al.
Molecular Psychiatry|February 25, 2009
Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autismF Laumonnier, C Shoubridge, C Antar, et al.
Nature|May 15, 1998
Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardationP Billuart, T Bienvenu, N Ronce, et al.
American Journal of Human Genetics|April 16, 1998
Mutations in the EXT1 and EXT2 genes in hereditary multiple exostosesW Wuyts, W Van Hul, K De Boulle, et al.
Nature Genetics|September 2, 1999
A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardationA Carrié, L Jun, T Bienvenu, et al.
Pageof 11

Showing results (91-100 of 103) with videos related to

Sort By:
Pageof 11
Annals of Internal Medicine|January 29, 2000
Resource use and survival of patients hospitalized with congestive heart failure: differences in care by specialty of the attending physician. SUPPORT Investigators. Study to Understand Prognoses and Preferences for Outcomes and Risks of TreatmentsA D Auerbach, M B Hamel, R B Davis, et al.
Journal of the American College of Cardiology|December 29, 2000
Patient characteristics associated with care by a cardiologist among adults hospitalized with severe congestive heart failure. SUPPORT Investigators. Study to Understand Prognoses and Preferences for Outcomes and Risks of TreatmentsA D Auerbach, M B Hamel, R M Califf, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlationsM R Nelen, H Kremer, I B Konings, et al.
Journal of Medical Genetics|November 25, 2003
A homozygous nonsense mutation in the fukutin gene causes a Walker-Warburg syndrome phenotypeD Beltrán-Valero de Bernabé, H van Bokhoven, E van Beusekom, et al.
American Journal of Medical Genetics|July 9, 1999
X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: the European XLMR consortiumV des Portes, C Beldjord, J Chelly, et al.
Circulation|August 26, 1998
Resuscitation preferences among patients with severe congestive heart failure: results from the SUPPORT project. Study to Understand Prognoses and Preferences for Outcomes and Risks of TreatmentsH M Krumholz, R S Phillips, M B Hamel, et al.
Molecular Psychiatry|February 25, 2009
Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autismF Laumonnier, C Shoubridge, C Antar, et al.
Nature|May 15, 1998
Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardationP Billuart, T Bienvenu, N Ronce, et al.
American Journal of Human Genetics|April 16, 1998
Mutations in the EXT1 and EXT2 genes in hereditary multiple exostosesW Wuyts, W Van Hul, K De Boulle, et al.
Nature Genetics|September 2, 1999
A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardationA Carrié, L Jun, T Bienvenu, et al.
Pageof 11