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International Archives of Allergy and Immunology
|
March 6, 2024
Pediatric Patients with Eosinophilic Esophagitis and Their Parents Identify Symptoms as the Most Important Treatment Outcome
Thea von Graffenried, Ekaterina Safroneeva, Christian Braegger, et al.
Scientific Reports
|
May 24, 2024
Improving the antinutritional profiles of common beans (Phaseolus vulgaris L.) moderately impacts carotenoid bioaccessibility but not mineral solubility
Katherine Alvarado-Ramos, Ángela Bravo-Nunez, Charlotte Halimi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 25, 2026
Racial and Socioeconomic Disparities in Blood Pressure Control Before and After Intracerebral Hemorrhage
Samuel Namian, Joel Smith, Sofia Constantinescu, et al.
European Journal of Medical Genetics
|
December 16, 2014
Molecular characterization of a cohort of 73 patients with infantile spasms syndrome
Nadia Boutry-Kryza, Audrey Labalme, Dorothee Ville, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 5, 2021
Evaluating next-generation sequencing in neuromuscular diseases with neonatal respiratory distress
Marie-Céline François-Heude, Ulrike Walther-Louvier, Caroline Espil-Taris, et al.
Brain & Development
|
June 5, 2018
Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations
Pauline Marzin, Cyril Mignot, Nathalie Dorison, et al.
Orphanet Journal of Rare Diseases
|
May 10, 2013
Natural history of Barth syndrome: a national cohort study of 22 patients
Charlotte Rigaud, Anne-Sophie Lebre, Renaud Touraine, et al.
Journal of Medical Genetics
|
August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations
N Bahi-Buisson, K Poirier, N Boddaert, et al.
Annals of Neurology
|
January 9, 2026
Longitudinal Trajectories of Brain Health Risk Factors Measured by the Brain Care Score and Risk of Stroke, Dementia, and Depression
Tamara N Kimball, Reinier W P Tack, Livia Parodi, et al.
European Journal of Human Genetics : EJHG
|
June 26, 2026
Decoding splicing variants in high-throughput sequencing: a functional validation approach integrating deep learning tools
Clément Hersent, Lise Larrieu, Patricia Fergelot, et al.
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Showing results (1281-1290 of 1,344) with videos related to
Sort By:
Page
of 135
International Archives of Allergy and Immunology
|
March 6, 2024
Pediatric Patients with Eosinophilic Esophagitis and Their Parents Identify Symptoms as the Most Important Treatment Outcome
Thea von Graffenried, Ekaterina Safroneeva, Christian Braegger, et al.
Scientific Reports
|
May 24, 2024
Improving the antinutritional profiles of common beans (Phaseolus vulgaris L.) moderately impacts carotenoid bioaccessibility but not mineral solubility
Katherine Alvarado-Ramos, Ángela Bravo-Nunez, Charlotte Halimi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 25, 2026
Racial and Socioeconomic Disparities in Blood Pressure Control Before and After Intracerebral Hemorrhage
Samuel Namian, Joel Smith, Sofia Constantinescu, et al.
European Journal of Medical Genetics
|
December 16, 2014
Molecular characterization of a cohort of 73 patients with infantile spasms syndrome
Nadia Boutry-Kryza, Audrey Labalme, Dorothee Ville, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 5, 2021
Evaluating next-generation sequencing in neuromuscular diseases with neonatal respiratory distress
Marie-Céline François-Heude, Ulrike Walther-Louvier, Caroline Espil-Taris, et al.
Brain & Development
|
June 5, 2018
Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations
Pauline Marzin, Cyril Mignot, Nathalie Dorison, et al.
Orphanet Journal of Rare Diseases
|
May 10, 2013
Natural history of Barth syndrome: a national cohort study of 22 patients
Charlotte Rigaud, Anne-Sophie Lebre, Renaud Touraine, et al.
Journal of Medical Genetics
|
August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations
N Bahi-Buisson, K Poirier, N Boddaert, et al.
Annals of Neurology
|
January 9, 2026
Longitudinal Trajectories of Brain Health Risk Factors Measured by the Brain Care Score and Risk of Stroke, Dementia, and Depression
Tamara N Kimball, Reinier W P Tack, Livia Parodi, et al.
European Journal of Human Genetics : EJHG
|
June 26, 2026
Decoding splicing variants in high-throughput sequencing: a functional validation approach integrating deep learning tools
Clément Hersent, Lise Larrieu, Patricia Fergelot, et al.
Page
of 135