Zobrazeno 1 - 3
of 3
pro vyhledávání: '"McKayla J Poppens"'
Publikováno v:
SAGE Open Medical Case Reports, Vol 12 (2024)
Poikilodermatous mycosis fungoides is a rare variant of cutaneous T-cell lymphoma that is often misdiagnosed given its diverse clinical presentation. Often diagnosed as vitiligo or morphea, poikilodermatous mycosis fungoides can be asymptomatic or pr
Externí odkaz:
https://doaj.org/article/c7235a0234074b0a9022e105acb5d0cf
Autor:
McKayla J. Poppens, Jacob T. Cain, Tyler B. Johnson, Katherine A. White, Samantha S. Davis, Rachel Laufmann, Alexander D. Kloth, Jill M. Weimer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Abstract Background CLN6-Batten disease is a rare neurodevelopmental disorder characterized pathologically by the accumulation of lysosomal storage material, glial activation and neurodegeneration, and phenotypically by loss of vision, motor coordina
Externí odkaz:
https://doaj.org/article/7b28cbfe339a47748e8ffc5fdc88fd71
Autor:
Rachel N. Laufmann, Katherine A. White, Jacob T. Cain, Alexander D. Kloth, Tyler B. Johnson, Jill M. Weimer, Samantha Davis, McKayla J. Poppens
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Background CLN6-Batten disease is a rare neurodevelopmental disorder characterized pathologically by the accumulation of lysosomal storage material, glial activation and neurodegeneration, and phenotypically by loss of vision, motor coordination, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0e4f89cfc71ac7ee6416173b5d6cb9c
https://pubmed.ncbi.nlm.nih.gov/30665444
https://pubmed.ncbi.nlm.nih.gov/30665444