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Anna L Mitchell

Showing results (21-30 of 61) with videos related to

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European Journal of Endocrinology|September 27, 2012
The role of functionally defective rare germline variants of sialic acid acetylesterase in autoimmune Addison's diseaseEarn H Gan, Katie MacArthur, Anna L Mitchell, et al.
European Thyroid Journal|August 9, 2017
Tremelimumab-Induced Graves HyperthyroidismEarn H Gan, Anna L Mitchell, Ruth Plummer, et al.
American Journal of Medical Genetics. Part A|February 24, 2011
Isolated skeletal malformations in a child with a small mosaic ring microduplication of 18 p11.21q11.2: genotype-phenotype correlationsThomas P Slavin, Kevin Kuruvilla, Christine A Curtis, et al.
Human Mutation|March 19, 2005
Bovine model of Marfan syndrome results from an amino acid change (c.3598G > A, p.E1200K) in a calcium-binding epidermal growth factor-like domain of fibrillin-1Annie C Singleton, Anna L Mitchell, Peter H Byers, et al.
European Journal of Endocrinology|January 18, 2023
Replication of association at the LPP and UBASH3A loci in a UK autoimmune Addison's disease cohortSophie Howarth, Georgina Sneddon, Kathleen R Allinson, et al.
Ophthalmic Genetics|February 17, 2016
Ocular manifestations of X-linked dominant FAM58A mutation in toe syndactyly, telecanthus, anogenital, and renal malformations ('STAR') syndromeFaruk H Orge, Suhail A Dar, Christie N Blackburn, et al.
Clinical Endocrinology|April 17, 2015
Spontaneous and tetracosactide-induced anti-ACTH antibodies in manEarn H Gan, Katie MacArthur, Anna L Mitchell, et al.
Clinical Endocrinology|July 30, 2017
Raising awareness of Graves' orbitopathy with early warning cardsAnna L Mitchell, Janis Hickey, Bijay Vaidya, et al.
Arthritis Care & Research|April 5, 2013
A 4-year-old Amish boy with weakness, arthritis, rash, verbal delay, and failure to thriveReut Gurion, Chinasa Nwankwo, Kabita Nanda, et al.
Connective Tissue Research|December 14, 2011
Characterization of tissue-specific and developmentally regulated alternative splicing of exon 64 in the COL5A1 geneAnna L Mitchell, LuAnn M Judis, Ulrike Schwarze, et al.
Pageof 7

Showing results (21-30 of 61) with videos related to

Sort By:
Pageof 7
European Journal of Endocrinology|September 27, 2012
The role of functionally defective rare germline variants of sialic acid acetylesterase in autoimmune Addison's diseaseEarn H Gan, Katie MacArthur, Anna L Mitchell, et al.
European Thyroid Journal|August 9, 2017
Tremelimumab-Induced Graves HyperthyroidismEarn H Gan, Anna L Mitchell, Ruth Plummer, et al.
American Journal of Medical Genetics. Part A|February 24, 2011
Isolated skeletal malformations in a child with a small mosaic ring microduplication of 18 p11.21q11.2: genotype-phenotype correlationsThomas P Slavin, Kevin Kuruvilla, Christine A Curtis, et al.
Human Mutation|March 19, 2005
Bovine model of Marfan syndrome results from an amino acid change (c.3598G > A, p.E1200K) in a calcium-binding epidermal growth factor-like domain of fibrillin-1Annie C Singleton, Anna L Mitchell, Peter H Byers, et al.
European Journal of Endocrinology|January 18, 2023
Replication of association at the LPP and UBASH3A loci in a UK autoimmune Addison's disease cohortSophie Howarth, Georgina Sneddon, Kathleen R Allinson, et al.
Ophthalmic Genetics|February 17, 2016
Ocular manifestations of X-linked dominant FAM58A mutation in toe syndactyly, telecanthus, anogenital, and renal malformations ('STAR') syndromeFaruk H Orge, Suhail A Dar, Christie N Blackburn, et al.
Clinical Endocrinology|April 17, 2015
Spontaneous and tetracosactide-induced anti-ACTH antibodies in manEarn H Gan, Katie MacArthur, Anna L Mitchell, et al.
Clinical Endocrinology|July 30, 2017
Raising awareness of Graves' orbitopathy with early warning cardsAnna L Mitchell, Janis Hickey, Bijay Vaidya, et al.
Arthritis Care & Research|April 5, 2013
A 4-year-old Amish boy with weakness, arthritis, rash, verbal delay, and failure to thriveReut Gurion, Chinasa Nwankwo, Kabita Nanda, et al.
Connective Tissue Research|December 14, 2011
Characterization of tissue-specific and developmentally regulated alternative splicing of exon 64 in the COL5A1 geneAnna L Mitchell, LuAnn M Judis, Ulrike Schwarze, et al.
Pageof 7