These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
296 related articles for article (PubMed ID: 35055176)
1. CRLF1 and CLCF1 in Development, Health and Disease. Crisponi L; Buers I; Rutsch F Int J Mol Sci; 2022 Jan; 23(2):. PubMed ID: 35055176 [TBL] [Abstract][Full Text] [Related]
2. Crisponi/Cold Induced Sweating Syndrome Type 1 With a Private Cytokine Receptor Like Factor 1 (CRLF1) Mutation in an Indian Family. Sahi PK; Mandal A; Persico I; Seth A; Crisponi L Indian Pediatr; 2020 Nov; 57(11):1075-1076. PubMed ID: 33231180 [No Abstract] [Full Text] [Related]
3. Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion. Schierz IAM; Serra G; Antona V; Persico I; Corsello G; Piro E Clin Dysmorphol; 2020 Jul; 29(3):141-143. PubMed ID: 32433043 [No Abstract] [Full Text] [Related]
4. Cold-induced sweating syndrome type 1, with a CRLF1 level mutation, previously associated with Crisponi syndrome. González Fernández D; Lázaro Pérez M; Santillán Garzón S; Alvarez Martínez V; Encinas Madrazo A; Fernández Toral J; Pérez Oliva N Dermatology; 2013; 227(2):126-9. PubMed ID: 24008591 [TBL] [Abstract][Full Text] [Related]
5. A new Turkish infant with clinical features of CS/CISS1 syndrome and homozygous CRLF1 mutation. Moortgat S; Benoit V; Deprez M; Charon A; Maystadt I Eur J Med Genet; 2014 Apr; 57(5):212-5. PubMed ID: 24613578 [TBL] [Abstract][Full Text] [Related]
15. A new case series of Crisponi syndrome in a Turkish family and review of the literature. Bayraktar-Tanyeri B; Hepokur M; Bayraktar S; Persico I; Crisponi L Clin Dysmorphol; 2017 Apr; 26(2):66-72. PubMed ID: 27977424 [TBL] [Abstract][Full Text] [Related]
16. Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa. Angius A; Uva P; Buers I; Oppo M; Puddu A; Onano S; Persico I; Loi A; Marcia L; Höhne W; Cuccuru G; Fotia G; Deiana M; Marongiu M; Atalay HT; Inan S; El Assy O; Smit LM; Okur I; Boduroglu K; Utine GE; Kılıç E; Zampino G; Crisponi G; Crisponi L; Rutsch F Am J Hum Genet; 2016 Jul; 99(1):236-45. PubMed ID: 27392078 [TBL] [Abstract][Full Text] [Related]
17. Novel CRLF1 gene mutation in a newborn infant diagnosed with Crisponi syndrome. Hakan N; Eminoglu FT; Aydin M; Zenciroglu A; Karadag NN; Dursun A; Okumus N; Ceylaner S Congenit Anom (Kyoto); 2012 Dec; 52(4):216-8. PubMed ID: 23181498 [TBL] [Abstract][Full Text] [Related]
18. Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line. Buers I; Schöning L; Tomas Loges N; Nitschke Y; Höben IM; Röpke A; Crisponi L; Omran H; Rutsch F Stem Cell Res; 2020 Jul; 46():101855. PubMed ID: 32512309 [TBL] [Abstract][Full Text] [Related]
19. Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders. Herholz J; Meloni A; Marongiu M; Chiappe F; Deiana M; Herrero CR; Zampino G; Hamamy H; Zalloum Y; Waaler PE; Crisponi G; Crisponi L; Rutsch F Eur J Hum Genet; 2011 May; 19(5):525-33. PubMed ID: 21326283 [TBL] [Abstract][Full Text] [Related]
20. Corneal alterations in Crisponi/CISS1 syndrome: A slit-lamp biomicroscopy and in vivo confocal microscopy corneal report. Agresta A; Fasciani R; Padua L; Petroni S; La Torraca I; Dickmann A; Zampino G; Caporossi A Ophthalmic Genet; 2017; 38(1):83-87. PubMed ID: 27054527 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]