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Skewed X-inactivation in a Female Carrier with X-linked Chronic Granulomatous Disease.
López-Hernández I, Deswarte C, Alcantara-Ortigoza MÁ, Saez-de-Ocariz MDM, Yamazaki-Nakashimada MA, Espinosa-Padilla SE, Bustamante J, Blancas-Galicia L. López-Hernández I, et al. Iran J Allergy Asthma Immunol. 2019 Aug 17;18(4):447-451. doi: 10.18502/ijaai.v18i4.1425. Iran J Allergy Asthma Immunol. 2019. PMID: 31522453 Free article. Review.
Successful stem cell transplantation in a child with chronic granulomatous disease associated with contiguous gene deletion syndrome and complicated by macrophage activation syndrome.
Scheffler-Mendoza SC, Yamazaki-Nakashimada MA, Olaya-Vargas A, Morin-Contreras A, Juárez-Echenique JC, Alcántara-Ortigoza MA, Zamora-Chávez A, Santos-Argumedo L, Blancas-Galicia L. Scheffler-Mendoza SC, et al. Clin Immunol. 2014 Oct;154(2):112-5. doi: 10.1016/j.clim.2014.07.004. Epub 2014 Jul 22. Clin Immunol. 2014. PMID: 25063445 No abstract available.
Expanding the clinical features of autoinflammation and phospholipase Cγ2-associated antibody deficiency and immune dysregulation by description of a novel patient.
Morán-Villaseñor E, Saez-de-Ocariz M, Torrelo A, Arostegui JI, Yamazaki-Nakashimada MA, Alcántara-Ortigoza MA, González-Del-Angel A, Velázquez-Aragón JA, López-Herrera G, Berrón-Ruiz L, García-Romero MT. Morán-Villaseñor E, et al. J Eur Acad Dermatol Venereol. 2019 Dec;33(12):2334-2339. doi: 10.1111/jdv.15918. Epub 2019 Oct 24. J Eur Acad Dermatol Venereol. 2019. PMID: 31465591
Hair pigment distribution changes after haematopoietic stem cell transplantation in Griscelli syndrome type 2.
Yamazaki-Nakashimada MA, Roldán-Marín R, Toussaint-Caire S, Olaya-Vargas A, Ramírez-Uribe N, Rivas-Larrauri F, Durán-McKinster C, Alcántara-Ortigoza MA, González-Del Angel A, Orozco-Covarrubias L, Scheffler-Mendoza S, Saez-de-Ocariz M. Yamazaki-Nakashimada MA, et al. J Eur Acad Dermatol Venereol. 2021 Jan;35(1):e53-e56. doi: 10.1111/jdv.16795. Epub 2020 Jul 22. J Eur Acad Dermatol Venereol. 2021. PMID: 32594618 No abstract available.
Screening of late-onset Pompe disease in a sample of Mexican patients with myopathies of unknown etiology: identification of a novel mutation in the acid alpha-glucosidase gene.
Alcántara-Ortigoza MA, González-del Angel A, Barrientos-Ríos R, Cupples C, Garrido-García LM, de León-Bojorge B, Alva-Chaire Adel C. Alcántara-Ortigoza MA, et al. J Child Neurol. 2010 Aug;25(8):1034-7. doi: 10.1177/0883073809356035. Epub 2010 Mar 29. J Child Neurol. 2010. PMID: 20350966
62 results