Zobrazeno 1 - 10
of 454
pro vyhledávání: '"Chronic infantile neurologic Cutaneous and articular syndrome"'
Autor:
Lackie, John
Publikováno v:
A Dictionary of Biomedicine, 2 ed., 2019.
Externí odkaz:
http://www.oxfordreference.com/view/10.1093/acref/9780191829116.001.0001/acref-9780191829116-e-1811
Akademický článek
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Autor:
Lackie, John
Publikováno v:
A Dictionary of Biomedicine, 1 ed., 2010.
Externí odkaz:
http://www.oxfordreference.com/view/10.1093/acref/9780199549351.001.0001/acref-9780199549351-e-1811
Autor:
Ryuta Nishikomori, Fumio Shiraga, Masayuki Hirano, Akiko Narita, Masahiro Yamamura, Hirotaka Okanobu, Toshio Heike, Jiro Seguchi, Mio Hosokawa, Yuki Morizane
Publikováno v:
Journal of Ophthalmic Inflammation and Infection
Background: Cryopyrin-associated periodic syndrome (CAPS) is a group of rare autoinflammatory diseases, and of these, chronic infantile neurologic, cutaneous, and articular/neonatal-onset multisystem inflammatory disease (CINCA/NOMID) syndrome has th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::439b74b0cbdb80a09f76adc99ce1bb69
https://pubmed.ncbi.nlm.nih.gov/26590045
https://pubmed.ncbi.nlm.nih.gov/26590045
Autor:
Gómez-Camello Á; Hospital Clinico Universitario San Cecilio, 18012 Granada, Espana., Ortego-Centeno N
Publikováno v:
Revista de neurologia [Rev Neurol] 2014 Jan 16; Vol. 58 (2), pp. 94-6.
Publikováno v:
Bone Dysplasias: An Atlas of Genetic Disorders of Skeletal Development
Chapter 11 covers CINCA (Chronic Infantile Neurologic Cutaneous and Articular) syndrome (MIM 607115), including major clinical findings, radiographic features, and differential diagnoses.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::746d9ad3ec2e81266f4865fa9f89bbd8
https://doi.org/10.1093/med/9780195396089.003.0011
https://doi.org/10.1093/med/9780195396089.003.0011
Publikováno v:
Europe PubMed Central
Descripcion de un caso de trastorno del movimiento hipercinetico en la enfermedad inflamatoria multisistemica de inicio neonatal o sindrome cronico infantil neurologico, cutaneo y articular.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::076236b3a7a79f7163a1c4c01ffec405
https://pubmed.ncbi.nlm.nih.gov/24399627
https://pubmed.ncbi.nlm.nih.gov/24399627
Autor:
Kyoko Yokoi, Sachiko Minamiguchi, Yoshitaka Honda, Mizuho Kobayashi, Satoru Kobayashi, Ryuta Nishikomori
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-6 (2021)
Abstract Background Cryopyrin-associated periodic syndrome (CAPS) is a life-long, autoinflammatory disease associated with a gain-of-function mutation in the nucleotide-binding domain, leucine-rich repeat family, pyrin domain containing 3 (NLRP3) gen
Externí odkaz:
https://doaj.org/article/94e3ffc48043492e98243a566a3e764c
Autor:
Milewska-Bobula B; Clinique du nourrisson, institut Monument, centre de santé de l'enfant, Varsovie, Pologne., Lipka B, Rowecka-Trzebicka K, Rostropowicz-Denisiewicz K, Romicka A, Witwicki JM
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie [Arch Pediatr] 1998 Oct; Vol. 5 (10), pp. 1094-7.
Autor:
Jenny Mae Samson, Dinoop Ravindran Menon, Prasanna K. Vaddi, Nazanin Kalani Williams, Joanne Domenico, Zili Zhai, Donald S. Backos, Mayumi Fujita
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Cyropyrin-associated periodic syndromes (CAPS) are clinically distinct syndromes that encompass a phenotypic spectrum yet are caused by alterations in the same gene, NLRP3. Many CAPS cases and other NLRP3-autoinflammatory diseases (NLRP3-AIDs) are di
Externí odkaz:
https://doaj.org/article/3a74afe64861427a9fc59e8e99d8cff3