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Anna L Mitchell

Showing results (51-60 of 61) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|December 22, 2019
Residual Adrenal Function in Autoimmune Addison's Disease-Effect of Dual Therapy With Rituximab and Depot TetracosactideCatherine Napier, Earn H Gan, Anna L Mitchell, et al.
The Journal of Clinical Endocrinology and Metabolism|December 9, 2014
Diagnosis of Graves' orbitopathy (DiaGO): results of a pilot study to assess the utility of an office tool for practicing endocrinologistsAnna L Mitchell, Linda Goss, Lemonia Mathiopoulou, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 27, 2014
High frequency of cytolytic 21-hydroxylase-specific CD8+ T cells in autoimmune Addison's disease patientsAmina Dawoodji, Ji-Li Chen, Dawn Shepherd, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2018
AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestationsRebecca J Darrah, Frank J Jacono, Neha Joshi, et al.
American Journal of Human Genetics|March 6, 2012
Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFBAndreas Zankl, Emma L Duncan, Paul J Leo, et al.
Thyroid : Official Journal of the American Thyroid Association|September 12, 2015
Future Research in Graves' Orbitopathy: From Priority Setting to Trial Design Through Patient and Public InvolvementPetros Perros, Colin M Dayan, A Jane Dickinson, et al.
Clinical Genetics|December 31, 2020
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2Yuri A Zarate, Katherine A Bosanko, Mary Ann Thomas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterationsEllen S Regalado, Lauren Mellor-Crummey, Julie De Backer, et al.
Clinical Endocrinology|September 24, 2021
SDHC phaeochromocytoma and paraganglioma: A UK-wide case seriesSophie T Williams, Prodromos Chatzikyriakou, Paul V Carroll, et al.
American Journal of Human Genetics|October 18, 2016
Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of ComplementInes Kapferer-Seebacher, Melanie Pepin, Roland Werner, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

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Pageof 7
The Journal of Clinical Endocrinology and Metabolism|December 22, 2019
Residual Adrenal Function in Autoimmune Addison's Disease-Effect of Dual Therapy With Rituximab and Depot TetracosactideCatherine Napier, Earn H Gan, Anna L Mitchell, et al.
The Journal of Clinical Endocrinology and Metabolism|December 9, 2014
Diagnosis of Graves' orbitopathy (DiaGO): results of a pilot study to assess the utility of an office tool for practicing endocrinologistsAnna L Mitchell, Linda Goss, Lemonia Mathiopoulou, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 27, 2014
High frequency of cytolytic 21-hydroxylase-specific CD8+ T cells in autoimmune Addison's disease patientsAmina Dawoodji, Ji-Li Chen, Dawn Shepherd, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2018
AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestationsRebecca J Darrah, Frank J Jacono, Neha Joshi, et al.
American Journal of Human Genetics|March 6, 2012
Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFBAndreas Zankl, Emma L Duncan, Paul J Leo, et al.
Thyroid : Official Journal of the American Thyroid Association|September 12, 2015
Future Research in Graves' Orbitopathy: From Priority Setting to Trial Design Through Patient and Public InvolvementPetros Perros, Colin M Dayan, A Jane Dickinson, et al.
Clinical Genetics|December 31, 2020
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2Yuri A Zarate, Katherine A Bosanko, Mary Ann Thomas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterationsEllen S Regalado, Lauren Mellor-Crummey, Julie De Backer, et al.
Clinical Endocrinology|September 24, 2021
SDHC phaeochromocytoma and paraganglioma: A UK-wide case seriesSophie T Williams, Prodromos Chatzikyriakou, Paul V Carroll, et al.
American Journal of Human Genetics|October 18, 2016
Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of ComplementInes Kapferer-Seebacher, Melanie Pepin, Roland Werner, et al.
Pageof 7