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G Altarescu

Showing results (11-20 of 24) with videos related to

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Human Reproduction (Oxford, England)|June 3, 2006
Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1G Altarescu, B Brooks, Y Kaplan, et al.
Fetal Diagnosis and Therapy|August 30, 2008
Polar body-based preimplantation genetic diagnosis for N-acetylglutamate synthase deficiencyG Altarescu, B Brooks, T Eldar-Geva, et al.
Muscle & Nerve|August 3, 2000
Cutaneous silent periods in patients with Fabry diseaseN A Syed, F Sandbrink, C A Luciano, et al.
Annals of Neurology|February 9, 2000
Profile of endothelial and leukocyte activation in Fabry patientsT DeGraba, S Azhar, F Dignat-George, et al.
Blood Cells, Molecules & Diseases|October 24, 2000
Comparative efficacy of dose regimens in enzyme replacement therapy of type I Gaucher diseaseG Altarescu, R Schiffmann, C C Parker, et al.
Stroke|July 7, 2001
Enhanced endothelium-dependent vasodilation in Fabry diseaseG Altarescu, D F Moore, R Pursley, et al.
Journal of Assisted Reproduction and Genetics|July 9, 2013
Familial haplotyping and embryo analysis for Preimplantation genetic diagnosis (PGD) using DNA microarrays: a proof of principle studyG Altarescu, D A Zeevi, S Zeligson, et al.
Reproductive Biomedicine Online|February 21, 2008
Successful polar body-based preimplantation genetic diagnosis for achondroplasiaG Altarescu, P Renbaum, B Brooks P, et al.
The Journal of Pediatrics|April 11, 2001
The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher's diseaseG Altarescu, S Hill, E Wiggs, et al.
Reproductive Biomedicine Online|May 13, 2014
Ovarian reserve and PGD treatment outcome in women with myotonic dystrophyN Srebnik, E J Margalioth, R Rabinowitz, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Human Reproduction (Oxford, England)|June 3, 2006
Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1G Altarescu, B Brooks, Y Kaplan, et al.
Fetal Diagnosis and Therapy|August 30, 2008
Polar body-based preimplantation genetic diagnosis for N-acetylglutamate synthase deficiencyG Altarescu, B Brooks, T Eldar-Geva, et al.
Muscle & Nerve|August 3, 2000
Cutaneous silent periods in patients with Fabry diseaseN A Syed, F Sandbrink, C A Luciano, et al.
Annals of Neurology|February 9, 2000
Profile of endothelial and leukocyte activation in Fabry patientsT DeGraba, S Azhar, F Dignat-George, et al.
Blood Cells, Molecules & Diseases|October 24, 2000
Comparative efficacy of dose regimens in enzyme replacement therapy of type I Gaucher diseaseG Altarescu, R Schiffmann, C C Parker, et al.
Stroke|July 7, 2001
Enhanced endothelium-dependent vasodilation in Fabry diseaseG Altarescu, D F Moore, R Pursley, et al.
Journal of Assisted Reproduction and Genetics|July 9, 2013
Familial haplotyping and embryo analysis for Preimplantation genetic diagnosis (PGD) using DNA microarrays: a proof of principle studyG Altarescu, D A Zeevi, S Zeligson, et al.
Reproductive Biomedicine Online|February 21, 2008
Successful polar body-based preimplantation genetic diagnosis for achondroplasiaG Altarescu, P Renbaum, B Brooks P, et al.
The Journal of Pediatrics|April 11, 2001
The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher's diseaseG Altarescu, S Hill, E Wiggs, et al.
Reproductive Biomedicine Online|May 13, 2014
Ovarian reserve and PGD treatment outcome in women with myotonic dystrophyN Srebnik, E J Margalioth, R Rabinowitz, et al.
Pageof 3