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Plos One|December 30, 2011
Evaluation of cellular phenotypes implicated in immunopathogenesis and monitoring immune reconstitution inflammatory syndrome in HIV/leprosy casesCarmem Beatriz Wagner Giacoia-Gripp, Anna Maria Sales, José Augusto da Costa Nery, et al.
Pediatric Emergency Care|February 17, 2025
Practice Variation in Urine Collection Among Emergency Department Providers in Pre-toilet-trained Children With Suspected Urinary Tract InfectionLucy M Wilson, Terry P Klassen, Tighe Crombie, et al.
American Journal of Medical Genetics|June 26, 2001
Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemiaK W Gripp, D M McDonald-McGinn, D La Rossa, et al.
AJNR. American Journal of Neuroradiology|September 3, 1998
Imaging studies in a unique familial dysmyelinating disorderK W Gripp, R A Zimmerman, Z J Wang, et al.
Ciencia & Saude Coletiva|December 3, 2025
Social validity of comprehensive sexuality education effects in the suburbs of the Federal District, Brazil: a case studyPatrícia de Souza Rezende Anderle, Dais Gonçalves Rocha, Flávia Mazitelli de Oliveira, et al.
Emerging Infectious Diseases|June 11, 2013
Clinical and therapeutic features of pulmonary nontuberculous mycobacterial disease, Brazil, 1993-2011Karla Gripp Couto de Mello, Fernanda C Queiroz Mello, Liamar Borga, et al.
Indian Journal of Dermatology, Venereology and Leprology|September 18, 2008
Contact with armadillos increases the risk of leprosy in Brazil: a case control studyP D Deps, B L Alves, C G Gripp, et al.
The Journal of Pediatrics|May 15, 1998
Identification of a genetic cause for isolated unilateral coronal synostosis: a unique mutation in the fibroblast growth factor receptor 3K W Gripp, D M McDonald-McGinn, K Gaudenz, et al.
JBRA Assisted Reproduction|December 26, 2024
Pregnancy in patients submitted to arterial embolization for uterine leiomyomasGustavo Santos Rainato, Marina Antonini E Silva, Jessica Abreu Ferreira Vaz de Melo, et al.
American Journal of Human Genetics|June 4, 2019
Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband SyndromeChristiane K Bauer, Pauline E Schneeberger, Fanny Kortüm, et al.
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