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Brain : a Journal of Neurology
|
November 29, 2011
Effect of growth hormone deficiency on brain structure, motor function and cognition
Emma A Webb, Michelle A O'Reilly, Jonathan D Clayden, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
April 16, 2026
Age-Specific Centiles for Fibroblast Growth Factor 23 and Its Associations with Mineral and Bone Metabolism in Healthy Children
Isabelle Piec, Andre Chu, Ben Nichols, et al.
American Journal of Medical Genetics. Part A
|
September 1, 2016
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations
Rebecca C Pollitt, Vrinda Saraff, Ann Dalton, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 23, 2017
Quantitative Brain MRI in Congenital Adrenal Hyperplasia: In Vivo Assessment of the Cognitive and Structural Impact of Steroid Hormones
Emma A Webb, Lucy Elliott, Dominic Carlin, et al.
Pediatric Endocrinology Reviews : PER
|
June 28, 2019
Karyotype - Phenotype Associations in Patients with Turner Syndrome
Iris D Noordman, Janiëlle Aem van der Velden, Henri Jlm Timmers, et al.
Plos Genetics
|
July 22, 2016
Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta
Wayne A Cabral, Masaki Ishikawa, Matthias Garten, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 22, 2017
Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect
Emma A Webb, Meena Balasubramanian, Nadja Fratzl-Zelman, et al.
Archives of Disease in Childhood
|
January 21, 2026
UK consensus guidelines for multidisciplinary care of children and young people with achondroplasia: a modified Delphi process
Toby P Candler, Kate Ali, Emma Bewick, et al.
Frontiers in Endocrinology
|
April 5, 2021
Quality of Life in Men With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Myrthe J M Verhees, Manon Engels, Paul N Span, et al.
Brain : a Journal of Neurology
|
September 12, 2013
ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies
Emma A Webb, Angham AlMutair, Daniel Kelberman, et al.
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Search research articles
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Showing results (11-20 of 20) with videos related to
Sort By:
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You have reached the last page of results.
This site can display upto 20 results.
Brain : a Journal of Neurology
|
November 29, 2011
Effect of growth hormone deficiency on brain structure, motor function and cognition
Emma A Webb, Michelle A O'Reilly, Jonathan D Clayden, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
April 16, 2026
Age-Specific Centiles for Fibroblast Growth Factor 23 and Its Associations with Mineral and Bone Metabolism in Healthy Children
Isabelle Piec, Andre Chu, Ben Nichols, et al.
American Journal of Medical Genetics. Part A
|
September 1, 2016
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations
Rebecca C Pollitt, Vrinda Saraff, Ann Dalton, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 23, 2017
Quantitative Brain MRI in Congenital Adrenal Hyperplasia: In Vivo Assessment of the Cognitive and Structural Impact of Steroid Hormones
Emma A Webb, Lucy Elliott, Dominic Carlin, et al.
Pediatric Endocrinology Reviews : PER
|
June 28, 2019
Karyotype - Phenotype Associations in Patients with Turner Syndrome
Iris D Noordman, Janiëlle Aem van der Velden, Henri Jlm Timmers, et al.
Plos Genetics
|
July 22, 2016
Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta
Wayne A Cabral, Masaki Ishikawa, Matthias Garten, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 22, 2017
Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect
Emma A Webb, Meena Balasubramanian, Nadja Fratzl-Zelman, et al.
Archives of Disease in Childhood
|
January 21, 2026
UK consensus guidelines for multidisciplinary care of children and young people with achondroplasia: a modified Delphi process
Toby P Candler, Kate Ali, Emma Bewick, et al.
Frontiers in Endocrinology
|
April 5, 2021
Quality of Life in Men With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Myrthe J M Verhees, Manon Engels, Paul N Span, et al.
Brain : a Journal of Neurology
|
September 12, 2013
ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies
Emma A Webb, Angham AlMutair, Daniel Kelberman, et al.
Page
of 2