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L Hubert

Showing results (51-60 of 69) with videos related to

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Journal of the American Medical Directors Association|June 3, 2024
Building a National Standard for Outreach and Assistance to At-Risk Patients During Large-Scale DisastersTamar Wyte-Lake, June Gin, Chad E Holmes, et al.
Annals of Internal Medicine|April 17, 2026
Rapid Evaluation of Artificial Intelligence Technology Used for Ambient Dictation in Primary Care: Comparing the Quality of Documentation of Artificial Intelligence-Generated and Human-Produced Clinical NotesAshok Reddy, Eric Gunnink, Chelle L Wheat, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 28, 2015
Two new cases of serine deficiency disorders treated with l-serineA Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Neuropediatrics|March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic studyS Romano, N Boddaert, I Desguerre, et al.
Protein Engineering|November 1, 1993
An improved linker for single-chain Fv with reduced aggregation and enhanced proteolytic stabilityM Whitlow, B A Bell, S L Feng, et al.
Fresenius' Journal of Analytical Chemistry|February 24, 2001
Multiparametric microsensor chips for screening applicationsR Ehret, W Baumann, M Brischwein, et al.
The Journal of Clinical Endocrinology and Metabolism|September 18, 2008
Chromosome 11p15 paternal isodisomy in focal forms of neonatal hyperinsulinismL Damaj, M le Lorch, V Verkarre, et al.
Orthopaedics & Traumatology, Surgery & Research : OTSR|November 1, 2011
Management of the stiff shoulder. A prospective multicenter comparative study of the six main techniques in use: 235 casesP Gleyze, P Clavert, P-H Flurin, et al.
JIMD Reports|February 23, 2013
Kinetic analyses guide the therapeutic decision in a novel form of moderate aromatic Acid decarboxylase deficiencyM Barth, V Serre, L Hubert, et al.
Journal of Inherited Metabolic Disease|March 12, 2009
Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B(12)V Valayannopoulos, L Hubert, J F Benoist, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
Journal of the American Medical Directors Association|June 3, 2024
Building a National Standard for Outreach and Assistance to At-Risk Patients During Large-Scale DisastersTamar Wyte-Lake, June Gin, Chad E Holmes, et al.
Annals of Internal Medicine|April 17, 2026
Rapid Evaluation of Artificial Intelligence Technology Used for Ambient Dictation in Primary Care: Comparing the Quality of Documentation of Artificial Intelligence-Generated and Human-Produced Clinical NotesAshok Reddy, Eric Gunnink, Chelle L Wheat, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 28, 2015
Two new cases of serine deficiency disorders treated with l-serineA Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Neuropediatrics|March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic studyS Romano, N Boddaert, I Desguerre, et al.
Protein Engineering|November 1, 1993
An improved linker for single-chain Fv with reduced aggregation and enhanced proteolytic stabilityM Whitlow, B A Bell, S L Feng, et al.
Fresenius' Journal of Analytical Chemistry|February 24, 2001
Multiparametric microsensor chips for screening applicationsR Ehret, W Baumann, M Brischwein, et al.
The Journal of Clinical Endocrinology and Metabolism|September 18, 2008
Chromosome 11p15 paternal isodisomy in focal forms of neonatal hyperinsulinismL Damaj, M le Lorch, V Verkarre, et al.
Orthopaedics & Traumatology, Surgery & Research : OTSR|November 1, 2011
Management of the stiff shoulder. A prospective multicenter comparative study of the six main techniques in use: 235 casesP Gleyze, P Clavert, P-H Flurin, et al.
JIMD Reports|February 23, 2013
Kinetic analyses guide the therapeutic decision in a novel form of moderate aromatic Acid decarboxylase deficiencyM Barth, V Serre, L Hubert, et al.
Journal of Inherited Metabolic Disease|March 12, 2009
Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B(12)V Valayannopoulos, L Hubert, J F Benoist, et al.
Pageof 7