Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Regina Zambrano"'
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
IntroductionRapid advancements in Next Generation Sequencing (NGS) and bioinformatics tools have allowed physicians to obtain genetic testing results in a more rapid, cost-effective, and comprehensive manner than ever before. Around 50% of pediatric
Externí odkaz:
https://doaj.org/article/512669708d0d4a6ea5a8630c6f66cc7b
Autor:
Christine Spaeth, Regina Zambrano
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101264- (2024)
Externí odkaz:
https://doaj.org/article/ad479733cac64890b7f7feea00c68962
Akademický článek
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Publikováno v:
SKIN The Journal of Cutaneous Medicine. 6:157-161
Leprosy is a chronic granulomatous infection caused by the bacteria Mycobacterium leprae. It can remain dormant in a patient without any symptoms until triggered by a stressor on the body. During the coronavirus disease 2019 (COVID-19) pandemic, a si
Publikováno v:
Revista Científica Hermes; out2023-mar2024, Vol. 34, p331-350, 20p
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 30, Iss 4, Pp 478-81 (2010)
Se presenta el caso de un paciente de 45 años de edad, de sexo masculino, con antecedentes de mieloma múltiple IgA y trasplante autólogo de células progenitoras, que consultó un cuadro de seis semanas de fiebre asociada a sintomatología constit
Externí odkaz:
https://doaj.org/article/90db822984ae44aeabcd3b027df4dba6
Publikováno v:
Cureus
We present a case of clear cell sarcoma (CCS) on the left large toe of an 80-year-old female. CCS, also known as “melanoma of soft parts,” is a rare soft tissue neoplasm that exhibits melanocytic differentiation. Most cases occur on the distal ex
Publikováno v:
American family physician. 102(4)
Autor:
Jeffrey W. Surcouf, Jessica Patrick-Esteve, Christian Lilje, Bianca Castellanos, Dana Rivera, Danielle Thompson, Michael Marble, Regina Zambrano, Pooja Desai, Yves Lacassie
Publikováno v:
Clinical Dysmorphology. 26:195-199
Noonan syndrome (NS) is an autosomal dominant disorder characterized by distinctive facial features, short neck, short stature, congenital heart defects, pectus deformities, and variable developmental delays. NS is genetically heterogeneous as pathog
Autor:
Regina Zambrano, Hannah Meddaugh
Publikováno v:
Clinical dysmorphology. 29(2)