Search research articles
Contact Us
Filters
Showing results (121-130 of 143) with videos related to
Page
of 15
Sort By:
Orphanet Journal of Rare Diseases
|
July 21, 2019
Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; a consensus statement from the European Reference Network for Congenital Malformations and Intellectual Disability
Jill Clayton-Smith, Rebecca Bromley, John Dean, et al.
Nature Neuroscience
|
January 22, 2019
Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projection
Wenjun Zhou, Yanlin He, Atteeq U Rehman, et al.
Nature Neuroscience
|
June 22, 2019
Author Correction: Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projection
Wenjun Zhou, Yanlin He, Atteeq U Rehman, et al.
The Journal of Sexual Medicine
|
November 6, 2010
International Society for Sexual Medicine's guidelines for the diagnosis and treatment of premature ejaculation
Stanley E Althof, Carmita H N Abdo, John Dean, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
|
October 30, 2014
Canadian hereditary angioedema guideline
Stephen Betschel, Jacquie Badiou, Karen Binkley, et al.
Nature Genetics
|
March 2, 2011
Mutations in the pre-replication complex cause Meier-Gorlin syndrome
Louise S Bicknell, Ernie M H F Bongers, Andrea Leitch, et al.
Nature Genetics
|
October 4, 2022
Gain-of-function mutations in KCNK3 cause a developmental disorder with sleep apnea
Janina Sörmann, Marcus Schewe, Peter Proks, et al.
American Journal of Human Genetics
|
February 1, 2020
Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism
Adam C Gunning, Klaudia Strucinska, Mikel Muñoz Oreja, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 11, 2024
A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorder
François Lecoquierre, A Mattijs Punt, Frédéric Ebstein, et al.
The Journal of Allergy and Clinical Immunology
|
September 10, 2004
Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema
Tom Bowen, Marco Cicardi, Henriette Farkas, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 143) with videos related to
Sort By:
Page
of 15
Orphanet Journal of Rare Diseases
|
July 21, 2019
Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; a consensus statement from the European Reference Network for Congenital Malformations and Intellectual Disability
Jill Clayton-Smith, Rebecca Bromley, John Dean, et al.
Nature Neuroscience
|
January 22, 2019
Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projection
Wenjun Zhou, Yanlin He, Atteeq U Rehman, et al.
Nature Neuroscience
|
June 22, 2019
Author Correction: Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projection
Wenjun Zhou, Yanlin He, Atteeq U Rehman, et al.
The Journal of Sexual Medicine
|
November 6, 2010
International Society for Sexual Medicine's guidelines for the diagnosis and treatment of premature ejaculation
Stanley E Althof, Carmita H N Abdo, John Dean, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
|
October 30, 2014
Canadian hereditary angioedema guideline
Stephen Betschel, Jacquie Badiou, Karen Binkley, et al.
Nature Genetics
|
March 2, 2011
Mutations in the pre-replication complex cause Meier-Gorlin syndrome
Louise S Bicknell, Ernie M H F Bongers, Andrea Leitch, et al.
Nature Genetics
|
October 4, 2022
Gain-of-function mutations in KCNK3 cause a developmental disorder with sleep apnea
Janina Sörmann, Marcus Schewe, Peter Proks, et al.
American Journal of Human Genetics
|
February 1, 2020
Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism
Adam C Gunning, Klaudia Strucinska, Mikel Muñoz Oreja, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 11, 2024
A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorder
François Lecoquierre, A Mattijs Punt, Frédéric Ebstein, et al.
The Journal of Allergy and Clinical Immunology
|
September 10, 2004
Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema
Tom Bowen, Marco Cicardi, Henriette Farkas, et al.
Page
of 15