Results 111 to 120 of about 96,208,754 (165)

Improved Outcomes in Congenital Insensitivity to Pain with Anhidrosis (CIPA) via a Multidisciplinary Clinic Model. [PDF]

J Clin Med
Shmueli M, Ling G, Elamour S, Weisel Y, Ben-Shimol S.   +4 more
europepmc   +1 more source

Living without pain: A 10-year study of congenital insensitivity to pain with anhidrosis. [PDF]

Pediatr Res
Klaitman SS, Ling G, Kristal E, David O, Elamour S, Hershkovitz E, Ling E.   +6 more
europepmc   +1 more source

Onychomadesis and phalanx osteolysis in congenital insensitivity to pain with anhidrosis

Rheumatology, 2020
Shu-Zhong, Liu, Xi, Zhou, An, Song, Yi-Peng, Wang, Yong, Liu   +4 more
openaire   +2 more sources

Recurrent Osteomyelitis in a Paediatric Patient with a Novel <i>NTRK1</i> Mutation: A Case Report on Congenital Insensitivity to Pain with Anhidrosis. [PDF]

Children (Basel)
Gasina L, Jain N, Viksne A, Ozols D, Kakar M, Bergmanis U.   +5 more
europepmc   +1 more source

Heterogeneity of clinical features and mutation analysis of NTRK1 in Han Chinese patients with congenital insensitivity to pain with anhidrosis. [PDF]

J Pain Res, 2019
Li N, Guo S, Wang Q, Duan G, Sun J, Liu Y, Zhang J, Wang C, Zhu C, Liu J, Zhang X.   +10 more
europepmc   +1 more source

Phenotypic and genotypic features of a pair of Chinese identical twins with congenital insensitivity to pain and anhidrosis: A case report. [PDF]

Medicine (Baltimore), 2018
Li N, Sun J, Guo S, Liu Y, Wang C, Zhu C, Zhang X.   +6 more
europepmc   +1 more source

Postoperative redislocation of the hip in a patient with congenital insensitivity to pain with anhidrosis: A case report and review of literature. [PDF]

World J Clin Cases, 2018
Wang R, Liu Y, Zhou YY, Wang JY, Xu ZJ, Chen SY, Wang QQ, Yuan P.   +7 more
europepmc   +1 more source

[Congenital insensitivity to pain with anhidrosis in the literature].

Archivos argentinos de pediatria, 2016
Pedro, Gargantilla, Emilio, Pintor
openaire   +1 more source

Humoral immunodeficiency in congenital insensitivity to pain with anhidrosis

neurogenetics, 2008
Congenital insensitivity to pain with anhidrosis (CIPA) is an autosomal recessive disorder caused by mutations in the neurotrophic tyrosine receptor kinase 1 (NTRK1) gene, which encodes the receptor for nerve growth factor. We report the clinical course of a 7-year-old girl with CIPA and proven NTRK1 mutation.
Kilic, SARA ŞEBNEM, Sarisozen, Bartu, Timmerman, Vincent, Baets, Jonathan, Rotthier, Annelies, Ozturk, Rifatcan   +5 more
openaire   +5 more sources