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Journal of Clinical Medicine
|
May 14, 2025
Cardiometabolic Risk in Chronic Spinal Cord Injury: A Systematic Review with Meta-Analysis and Temporal and Geographical Trends
Gary J Farkas, Lizeth J Caldera, Daniel D Hodgkiss, et al.
Pituitary
|
November 16, 2019
A Brazilian multicentre study evaluating pregnancies induced by cabergoline in patients harboring prolactinomas
B G Sant' Anna, N R C Musolino, M R Gadelha, et al.
The Journal of Pediatrics
|
March 13, 2017
Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability
Solveig Heide, Boris Keren, Thierry Billette de Villemeur, et al.
European Journal of Human Genetics : EJHG
|
February 9, 2017
Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome
Angélique Quartier, Hélène Poquet, Brigitte Gilbert-Dussardier, et al.
European Journal of Medical Genetics
|
July 21, 2015
From splitting GLUT1 deficiency syndromes to overlapping phenotypes
Marie Hully, Sandrine Vuillaumier-Barrot, Christiane Le Bizec, et al.
Orphanet Journal of Rare Diseases
|
December 14, 2012
Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms
David Cheillan, Marie Joncquel-Chevalier Curt, Gilbert Briand, et al.
Molecular Genetics and Metabolism
|
October 5, 2013
Creatine and guanidinoacetate reference values in a French population
Marie Joncquel-Chevalier Curt, David Cheillan, Gilbert Briand, et al.
Heart Rhythm
|
November 16, 2025
Prominent U-waves without QT prolongation in X-linked creatine transporter deficiency caused by SLC6A8 variants
Antoine Delinière, Chloé Mulatier, David Cheillan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 9, 2021
Machine Learning-based Prediction Model for Treatment of Acromegaly With First-generation Somatostatin Receptor Ligands
Luiz Eduardo Wildemberg, Aline Helen da Silva Camacho, Renan Lyra Miranda, et al.
Nature Genetics
|
April 23, 2013
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
Karine Poirier, Nicolas Lebrun, Loic Broix, et al.
Page
of 67
Search research articles
Search
Showing results (641-650 of 669) with videos related to
Sort By:
Page
of 67
Journal of Clinical Medicine
|
May 14, 2025
Cardiometabolic Risk in Chronic Spinal Cord Injury: A Systematic Review with Meta-Analysis and Temporal and Geographical Trends
Gary J Farkas, Lizeth J Caldera, Daniel D Hodgkiss, et al.
Pituitary
|
November 16, 2019
A Brazilian multicentre study evaluating pregnancies induced by cabergoline in patients harboring prolactinomas
B G Sant' Anna, N R C Musolino, M R Gadelha, et al.
The Journal of Pediatrics
|
March 13, 2017
Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability
Solveig Heide, Boris Keren, Thierry Billette de Villemeur, et al.
European Journal of Human Genetics : EJHG
|
February 9, 2017
Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome
Angélique Quartier, Hélène Poquet, Brigitte Gilbert-Dussardier, et al.
European Journal of Medical Genetics
|
July 21, 2015
From splitting GLUT1 deficiency syndromes to overlapping phenotypes
Marie Hully, Sandrine Vuillaumier-Barrot, Christiane Le Bizec, et al.
Orphanet Journal of Rare Diseases
|
December 14, 2012
Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms
David Cheillan, Marie Joncquel-Chevalier Curt, Gilbert Briand, et al.
Molecular Genetics and Metabolism
|
October 5, 2013
Creatine and guanidinoacetate reference values in a French population
Marie Joncquel-Chevalier Curt, David Cheillan, Gilbert Briand, et al.
Heart Rhythm
|
November 16, 2025
Prominent U-waves without QT prolongation in X-linked creatine transporter deficiency caused by SLC6A8 variants
Antoine Delinière, Chloé Mulatier, David Cheillan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 9, 2021
Machine Learning-based Prediction Model for Treatment of Acromegaly With First-generation Somatostatin Receptor Ligands
Luiz Eduardo Wildemberg, Aline Helen da Silva Camacho, Renan Lyra Miranda, et al.
Nature Genetics
|
April 23, 2013
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
Karine Poirier, Nicolas Lebrun, Loic Broix, et al.
Page
of 67