Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Graham‐Little Piccardi Lassueur syndrome"'
Publikováno v:
JAAD Case Reports, Vol 52, Iss , Pp 49-51 (2024)
Externí odkaz:
https://doaj.org/article/619a3316517142c380387c9e7c1e08b5
Publikováno v:
Romanian Medical Journal, Vol 70, Iss 2, Pp 98-101 (2023)
Objectives. We present a very rare case of incomplete Graham-Little-Piccardi-Lassueur syndrome (GLPLS) overlap with Mixed Connective Tissue Disease (MCTD) versus Multiple Autoimmune Syndrome (MAS). Case Presentation. A 53- year-old female with a long
Externí odkaz:
https://doaj.org/article/83a495a4237248f2a749371019bff584
Autor:
Diego Soto-García, MD, Carlos Feal-Cortizas, MD, Carlos Álvarez, MD, Carmen Couselo-Rodríguez, MD, Sandra Martínez-Fernández, MD, Ángeles Flórez, PhD
Publikováno v:
JAAD Case Reports, Vol 23, Iss , Pp 128-132 (2022)
Externí odkaz:
https://doaj.org/article/e49fa0a47dfb4c838c474a23dda3fe2f
Akademický článek
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Publikováno v:
Acta Medica Bulgarica, Vol 47, Iss 4, Pp 58-62 (2020)
Graham-Little-Piccardi-Lassueur syndrome (GLPLS) is a rare syndrome characterized by the triad of cicatricial alopecia of the scalp, non-cicatricial alopecia of the axilla and groin and follicular lichen planus eruptions on the trunk and extremities.
Externí odkaz:
https://doaj.org/article/251079f65f894488830fc69ca07c1d2d
Autor:
Mariachiara Arisi, Alessandra Gelmetti, Arianna Zanca, Mariateresa Rossi, Luisa Lorenzi, Paolo Incardona, Piergiacomo Calzavara-Pinton, Marina Venturini
Publikováno v:
Dermatology and Therapy, Vol 10, Iss 4, Pp 887-892 (2020)
Abstract Graham Little-Piccardi-Lassueur syndrome (GLPLS) is a rare variant of lichen planopilaris, characterized by a triad of clinical signs including follicular spinous papules on the body area, scarring alopecia of the scalp and non-scarring alop
Externí odkaz:
https://doaj.org/article/5866604401fc4c8486cc6385678c4380
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract Graham‐Little Piccardi Lassueur Syndrome (GLPLS) is a rare variant of lichen planopilaris (LPP) which characterized by triad of fibrosing alopecia of the scalp, non‐fibrosing alopecia of the axilla and groin, and a follicular spinous pap
Externí odkaz:
https://doaj.org/article/8d61a89e86a54ef089996f3135fa1334
Publikováno v:
Acta Medica Bulgarica, Vol 47, Iss 4, Pp 58-62 (2020)
Graham-Little-Piccardi-Lassueur syndrome (GLPLS) is a rare syndrome characterized by the triad of cicatricial alopecia of the scalp, non-cicatricial alopecia of the axilla and groin and follicular lichen planus eruptions on the trunk and extremities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cc930b6a6d6163c2c966dbe5c027d61
https://doi.org/10.2478/amb-2020-0047
https://doi.org/10.2478/amb-2020-0047
Autor:
Luisa Lorenzi, Arianna Zanca, Alessandra Gelmetti, Marina Venturini, Mariachiara Arisi, Mariateresa Rossi, Paolo Incardona, Piergiacomo Calzavara-Pinton
Publikováno v:
Dermatology and Therapy
Dermatology and Therapy, Vol 10, Iss 4, Pp 887-892 (2020)
Dermatology and Therapy, Vol 10, Iss 4, Pp 887-892 (2020)
Graham Little-Piccardi-Lassueur syndrome (GLPLS) is a rare variant of lichen planopilaris, characterized by a triad of clinical signs including follicular spinous papules on the body area, scarring alopecia of the scalp and non-scarring alopecia of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b7c6ff4611a3033e72fb00771803bab
http://europepmc.org/articles/PMC7367984
http://europepmc.org/articles/PMC7367984
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Graham‐Little Piccardi Lassueur Syndrome (GLPLS) is a rare variant of lichen planopilaris (LPP) which characterized by triad of fibrosing alopecia of the scalp, non‐fibrosing alopecia of the axilla and groin, and a follicular spinous papule over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0561a2b79d67334136dee861a178dbc5
http://europepmc.org/articles/PMC8418680
http://europepmc.org/articles/PMC8418680