Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Carola Duran McKinster"'
Akademický článek
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Autor:
Sara Elva Espinosa-Padilla, Selma Scheffler-Mendoza, Marco Antonio Yamazaki-Nakashimada, Saúl Oswaldo Lugo-Reyes, Carola Duran McKinster, Lina Maria Castano-Jaramillo, Maria Del Mar Saez-de-Ocariz Gutierrez, Mario E Cruz Muñoz
Publikováno v:
Scandinavian Journal of Immunology. 93
Griscelli syndrome (GS) is a rare autosomal recessive disease with characteristic pigment distribution, and there are currently 3 types according to the underlying genetic defect and clinical features. We present the case of a girl born from consangu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1861eab827e544d86f083d07eaba6cb
https://doi.org/10.1111/sji.13034
https://doi.org/10.1111/sji.13034
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Ramon Ruiz-Maldonado, Carola Duran-Mckinster, Raquel Lara-Carpio, Carolina Palacios-Lopez, Marimar Sáez-de-Ocariz, Luz Orozco-Covarrubias
Publikováno v:
Pediatric Dermatology. 30:706-711
Dermoid cysts (DCs) are benign cutaneous tumors that tend to persist and grow. The aim of this study was to examine the clinicopathologic features of congenital DCs. We present a case series of 75 children with a clinicopathologic diagnosis of DC. Se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05f0097414f289236e903d71174612ba
https://doi.org/10.1111/pde.12080
https://doi.org/10.1111/pde.12080
Pediatric Skin of Color is the first textbook devoted to the issues of pediatric skin of color. In 2052, more than fifty percent of the United States will be of color, and currently seventy percent of the world's population is termed of color. T
Autor:
Ramon Ruiz-Maldonado, Carola Duran-Mckinster, Marimar Sáez-de-Ocariz, Rolando Elias Julián-Gónzalez, Carolina Palacios-Lopez, Luz Orozco-Covarrubias
Publikováno v:
Pediatric Dermatology. 29:580-583
The common manifestations of atopic dermatitis (AD) appear sequentially with involvement of the cheeks in infancy, flexural extremities in childhood, and hands in adulthood. Although less common clinical manifestations are well described, they have n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fc1bfc2064d57ce28d2f7d32e4153f1
https://doi.org/10.1111/j.1525-1470.2012.01739.x
https://doi.org/10.1111/j.1525-1470.2012.01739.x
Autor:
Paola Valenzuela-León, Carola Duran-McKinster, Marco Antonio Yamazaki-Nakashimada, Francisco Rivas-Larrauri, Leopoldo Santos-Argumedo, Noé Ramírez-Alejo, Julio C. Alcántara-Montiel, Rosaura Hernández-Rivas, Leticia Cedillo-Barrón
Publikováno v:
Clinical immunology (Orlando, Fla.). 160(2)
NF-κB essential modulator (NEMO) is a component of the IKK complex, which participates in the activation of the NF-κB pathway. Hypomorphic mutations in the IKBKG gene result in different forms of anhidrotic ectodermal dysplasia with immunodeficienc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19efb3a24c5c8b3b2b47b5a43dac5f0d
https://pubmed.ncbi.nlm.nih.gov/26117626
https://pubmed.ncbi.nlm.nih.gov/26117626
Autor:
Ramon Ruiz-Maldonado, Carola Duran-Mckinster, Helena Vidaurri-de la Cruz, Lourdes Tamayo-Sanchez, María De La Luz Orozco-Covarrubias
Publikováno v:
Pediatric Dermatology. 21:432-439
Of the patients with epidermal nevi, 10-18% may have disorders of the eye, nervous, and musculoskeletal systems. A predisposition to malignant neoplasms in ectodermal and mesodermal structures may also be found. There are six different epidermal nevu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a429d108fd9f4066ba53e76fa0fe8931
https://doi.org/10.1111/j.0736-8046.2004.21402.x
https://doi.org/10.1111/j.0736-8046.2004.21402.x
Autor:
Ramon Ruiz-Maldonado, Daniel Carrasco-Daza, Marimar Saez-De-Ocaris, Carola Duran-Mckinster, Luz Orozco-Covarrubias, Carolina Palacios-Lopez, Rolando Elias Julián-Gónzalez
Publikováno v:
Pediatric Dermatology. 28:460-462
Congenital cutaneous angioleiomyoma is an extremely rare benign smooth muscle tumor. We present a case of a firm, painful subcutaneous mass noticed at birth on the left leg that on surgical excision proved to be an angioleiomyoma. Prognosis is good,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1ad6874d10b15be185ea51047529e58
https://doi.org/10.1111/j.1525-1470.2010.01290.x
https://doi.org/10.1111/j.1525-1470.2010.01290.x
Autor:
Veronica, Narvaez-Rosales, Marimar Saez, de-Ocariz, Daniel, Carrasco-Daza, Brenda, Ramirez-Davila, Luz, Orozco-Covarrubias, Carola, Duran-McKinster, Carolina, Palacios-Lopez
Publikováno v:
International journal of dermatology. 52(10)
Transient myeloproliferative disorder (TMD) affects up to 10% of patients with Down syndrome (DS). A small proportion of newborns are asymptomatic and only manifest circulating blast cells, with or without leukocytosis, while others present with hepa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c6badcb957e1712055f6cdcf09ca1d0
https://pubmed.ncbi.nlm.nih.gov/23046498
https://pubmed.ncbi.nlm.nih.gov/23046498