Search research articles
Contact Us
Filters
Showing results (871-880 of 947) with videos related to
Page
of 95
Sort By:
The Journal of Clinical Endocrinology and Metabolism
|
June 14, 2014
Increased visceral adiposity and cortisol to cortisone ratio in adults with congenital lifetime isolated GH deficiency
Elenilde Gomes-Santos, Roberto Salvatori, Thiago O Ferrão, et al.
The Journal of Investigative Dermatology
|
November 12, 2021
Differences in Clinical Features and Comorbid Burden between HLA-C∗06:02 Carrier Groups in >9,000 People with Psoriasis
Konstantinos Douroudis, Ravi Ramessur, Ines A Barbosa, et al.
Life Science Alliance
|
August 1, 2022
Novel <i>DNM1L</i> variants impair mitochondrial dynamics through divergent mechanisms
Kelsey A Nolden, John M Egner, Jack J Collier, et al.
Arquivos Brasileiros De Cardiologia
|
October 23, 2024
Association between Arterial Stiffness and Higher Burden of Atrial Arrhythmia in Elderly Hypertensive Patients without Atrial Fibrillation
João Gabriel B Lage, Alexandre L Bortolotto, Luiz A Bortolotto, et al.
Endocrine Connections
|
August 14, 2014
Liver status in congenital, untreated, isolated GH deficiency
Rachel D C A Diniz, Renata M Souza, Roberto Salvatori, et al.
JCI Insight
|
February 22, 2023
Development of antidrug antibodies against adalimumab maps to variation within the HLA-DR peptide-binding groove
Teresa Tsakok, Jake Saklatvala, Theo Rispens, et al.
American Journal of Human Genetics
|
December 3, 2016
Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number
Kyle Thompson, Homa Majd, Cristina Dallabona, et al.
American Journal of Human Genetics
|
October 4, 2016
Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number
Kyle Thompson, Homa Majd, Cristina Dallabona, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 24, 2013
Isolated GH deficiency due to a GHRH receptor mutation causes hip joint problems and genu valgum, and reduces size but not density of trabecular and mixed bone
Carlos C Epitácio-Pereira, Gabriella M F Silva, Roberto Salvatori, et al.
Brain : a Journal of Neurology
|
October 30, 2015
LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population
Monika Oláhová, Steven A Hardy, Julie Hall, et al.
Page
of 95
Search research articles
Search
Showing results (871-880 of 947) with videos related to
Sort By:
Page
of 95
The Journal of Clinical Endocrinology and Metabolism
|
June 14, 2014
Increased visceral adiposity and cortisol to cortisone ratio in adults with congenital lifetime isolated GH deficiency
Elenilde Gomes-Santos, Roberto Salvatori, Thiago O Ferrão, et al.
The Journal of Investigative Dermatology
|
November 12, 2021
Differences in Clinical Features and Comorbid Burden between HLA-C∗06:02 Carrier Groups in >9,000 People with Psoriasis
Konstantinos Douroudis, Ravi Ramessur, Ines A Barbosa, et al.
Life Science Alliance
|
August 1, 2022
Novel <i>DNM1L</i> variants impair mitochondrial dynamics through divergent mechanisms
Kelsey A Nolden, John M Egner, Jack J Collier, et al.
Arquivos Brasileiros De Cardiologia
|
October 23, 2024
Association between Arterial Stiffness and Higher Burden of Atrial Arrhythmia in Elderly Hypertensive Patients without Atrial Fibrillation
João Gabriel B Lage, Alexandre L Bortolotto, Luiz A Bortolotto, et al.
Endocrine Connections
|
August 14, 2014
Liver status in congenital, untreated, isolated GH deficiency
Rachel D C A Diniz, Renata M Souza, Roberto Salvatori, et al.
JCI Insight
|
February 22, 2023
Development of antidrug antibodies against adalimumab maps to variation within the HLA-DR peptide-binding groove
Teresa Tsakok, Jake Saklatvala, Theo Rispens, et al.
American Journal of Human Genetics
|
December 3, 2016
Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number
Kyle Thompson, Homa Majd, Cristina Dallabona, et al.
American Journal of Human Genetics
|
October 4, 2016
Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number
Kyle Thompson, Homa Majd, Cristina Dallabona, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 24, 2013
Isolated GH deficiency due to a GHRH receptor mutation causes hip joint problems and genu valgum, and reduces size but not density of trabecular and mixed bone
Carlos C Epitácio-Pereira, Gabriella M F Silva, Roberto Salvatori, et al.
Brain : a Journal of Neurology
|
October 30, 2015
LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population
Monika Oláhová, Steven A Hardy, Julie Hall, et al.
Page
of 95