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Diabetes/Metabolism Research and Reviews
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February 25, 2024
Adherence to an energy-restricted Mediterranean diet is associated with the presence and burden of carotid atherosclerosis in people with type 1 diabetes
Tonet Serés-Noriega, Clara Viñals, Verónica Perea, et al.
Reproductive Health
|
September 22, 2017
Clinical review of 24-35 year olds conceived with and without in vitro fertilization: study protocol
Sharon Lewis, Joanne Kennedy, David Burgner, et al.
Diabetes Research and Clinical Practice
|
June 21, 2025
Hepatic steatosis with significant fibrosis is associated with preclinical carotid atherosclerosis in patients with type 1 diabetes
Maria Claro, Clara Viñals, Marga Giménez, et al.
Neurology
|
April 17, 2015
Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR
Richard J Leventer, Thomas Scerri, Ashley P L Marsh, et al.
Human Molecular Genetics
|
January 12, 2013
Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and puberty
David E Godler, Yoshimi Inaba, Elva Z Shi, et al.
Diabetes Research and Clinical Practice
|
August 28, 2021
Weight gain following pancreas transplantation in type 1 diabetes is associated with a worse glycemic profile: A retrospective cohort study
Antonio J Amor, Aida Casas, Adriana Pané, et al.
Scientific Reports
|
October 27, 2019
Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing
Charles H Hensel, Rena J Vanzo, Megan M Martin, et al.
Neurology. Genetics
|
August 12, 2024
Inherited <i>PURA</i> Pathogenic Variant Associated With a Mild Neurodevelopmental Disorder
Michael S Hildebrand, Ruth O Braden, Mariana L Lauretta, et al.
Research in Developmental Disabilities
|
September 30, 2022
Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disorders
Marta Arpone, Lesley Bretherton, David J Amor, et al.
Clinical Chemistry
|
January 12, 2012
Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study
David E Godler, Howard R Slater, Quang M Bui, et al.
Page
of 43
Search research articles
Search
Showing results (271-280 of 430) with videos related to
Sort By:
Page
of 43
Diabetes/Metabolism Research and Reviews
|
February 25, 2024
Adherence to an energy-restricted Mediterranean diet is associated with the presence and burden of carotid atherosclerosis in people with type 1 diabetes
Tonet Serés-Noriega, Clara Viñals, Verónica Perea, et al.
Reproductive Health
|
September 22, 2017
Clinical review of 24-35 year olds conceived with and without in vitro fertilization: study protocol
Sharon Lewis, Joanne Kennedy, David Burgner, et al.
Diabetes Research and Clinical Practice
|
June 21, 2025
Hepatic steatosis with significant fibrosis is associated with preclinical carotid atherosclerosis in patients with type 1 diabetes
Maria Claro, Clara Viñals, Marga Giménez, et al.
Neurology
|
April 17, 2015
Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR
Richard J Leventer, Thomas Scerri, Ashley P L Marsh, et al.
Human Molecular Genetics
|
January 12, 2013
Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and puberty
David E Godler, Yoshimi Inaba, Elva Z Shi, et al.
Diabetes Research and Clinical Practice
|
August 28, 2021
Weight gain following pancreas transplantation in type 1 diabetes is associated with a worse glycemic profile: A retrospective cohort study
Antonio J Amor, Aida Casas, Adriana Pané, et al.
Scientific Reports
|
October 27, 2019
Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing
Charles H Hensel, Rena J Vanzo, Megan M Martin, et al.
Neurology. Genetics
|
August 12, 2024
Inherited <i>PURA</i> Pathogenic Variant Associated With a Mild Neurodevelopmental Disorder
Michael S Hildebrand, Ruth O Braden, Mariana L Lauretta, et al.
Research in Developmental Disabilities
|
September 30, 2022
Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disorders
Marta Arpone, Lesley Bretherton, David J Amor, et al.
Clinical Chemistry
|
January 12, 2012
Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study
David E Godler, Howard R Slater, Quang M Bui, et al.
Page
of 43