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Chilblains outbreak during COVID-19 pandemic: A Type-I interferonopathy?
Mensa-Vilaró A, Vicente A, Español-Rego M, Antón J, Fabregat V, Fortuny C, González EA, Fumadó V, González-Roca E, Jou C, Plaza S, Mosquera JM, Yagüe J, Prat C, Pascal M, Juan M, Arostegui JI, Baselga E, Alsina L. Mensa-Vilaró A, et al. Among authors: prat c. Pediatr Allergy Immunol. 2022 Oct;33(10):e13860. doi: 10.1111/pai.13860. Pediatr Allergy Immunol. 2022. PMID: 36282139 Free PMC article. No abstract available.
Linear juvenile dermatomyositis: A segmental manifestation.
Alamon-Reig F, Sánchez-Puigdollers A, Juan-Carpena G, Sanhueza T, Bosquez D, Prat C, Vicente-Villa A, Baselga E. Alamon-Reig F, et al. Among authors: prat c. Pediatr Dermatol. 2023 Jul-Aug;40(4):747-748. doi: 10.1111/pde.15291. Epub 2023 Mar 17. Pediatr Dermatol. 2023. PMID: 36932640
Silvery hair and neurologic impairment in a 21-month-old boy.
Rusiñol L, Baselga E, Garcia-Garcia A, Armstrong J, Prat C, Vicente A, Ivars M. Rusiñol L, et al. Among authors: prat c. J Dtsch Dermatol Ges. 2023 Sep;21(9):1043-1045. doi: 10.1111/ddg.15109. Epub 2023 Jun 9. J Dtsch Dermatol Ges. 2023. PMID: 37293827 No abstract available.
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies.
Brooks D, Burke E, Lee S, Eble TN, O'Leary M, Osei-Owusu I, Rehm HL, Dhar SU, Emrick L, Bick D, Nehrebecky M, Macnamara E, Casas-Alba D, Armstrong J, Prat C, Martínez-Monseny AF, Palau F, Liu P, Adams D; Undiagnosed Diseases Network; Lalani S, Rosenfeld JA, Burrage LC. Brooks D, et al. Among authors: prat c. Hum Genet. 2024 Mar;143(3):279-291. doi: 10.1007/s00439-024-02657-2. Epub 2024 Mar 7. Hum Genet. 2024. PMID: 38451290
Connaissez-vous le FOP ?
Picart C, Prat C, Marie C, Cudennec T, Pépin M. Picart C, et al. Among authors: prat c. Soins Gerontol. 2023 Jul-Aug;28(162):47-48. doi: 10.1016/j.sger.2023.04.012. Epub 2023 Jun 7. Soins Gerontol. 2023. PMID: 37481292 French. No abstract available.
229 results