Results 81 to 90 of about 108,138 (122)

Particularidades de la erupción dentaria en individuos infanto-juveniles con enfermedades endocrinas frecuentes

Medicentro, 2019
Introducción: la erupción de los dientes es un fenómeno biológico de interés médico y social. Este puede ser alterado por causas congénitas y adquiridas.
Lesdy Autié Méndez, Olga Lidia Véliz Concepción, Armando San Miguel Pentón, Julieta García Sáez   +3 more
doaj  

Fallo de medro como manifestación inicial de hiperplasia suprarrenal congénita por déficit de 21-hidroxilasa

La hiperplasia suprarrenal congénita por deficiencia de 21-hidroxilasa constituye la causa más frecuente de alteración de la esteroidogénesis suprarrenal y representa una urgencia endocrinológica en el período neonatal cuando se presenta con pérdida de ...
María Camila Rodriguez Acosta, Luis Felipe Bonfante Villalobos, Lina Marcela Sanchez Ibarra, Daniela Gonzalez Sierra, Andrea Carolina Meza Castellón, Daniel Josué Naranjo Coronel   +5 more
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Hiperplasia adrenal congênita: avanços diagnósticos e terapêuticos [PDF]

Introduction: Congenital adrenal hyperplasia (CAH) is a set of autosomal recessive pathology, described by the production of steroids in the adrenal cortex, frequently caused by deficiency of the 21-hydroxylase enzyme.
Pessoa, Julyana Eulália Pereira, Andrade, Anna Beatriz Ramalho Cavalcanti de, Cavalcante , Gabriela da Rocha Tenório, Badin , Larissa Milena Nogarolli, Júnior , Wilson Moraes Amaral, Casado, Ana Paula Barbosa, d’Oliveira , Ruane Clemente Costa, Galindo, Marcos Vinícius Lima, Góes , Bruno Oliveira, Nobre, Paulo Vytor Cardoso, Rocha, Monique Fany de Oliveira, Gama, Hulfshoff Damasceno, Gama, Guilherme Alves Damasceno Texeira   +12 more
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Brazilian Guidelines of Hypertension - 2020. [PDF]

Arq Bras Cardiol, 2021
Barroso WKS, Rodrigues CIS, Bortolotto LA, Mota-Gomes MA, Brandão AA, Feitosa ADM, Machado CA, Poli-de-Figueiredo CE, Amodeo C, Mion Júnior D, Barbosa ECD, Nobre F, Guimarães ICB, Vilela-Martin JF, Yugar-Toledo JC, Magalhães MEC, Neves MFT, Jardim PCBV, Miranda RD, Póvoa RMDS, Fuchs SC, Alessi A, Lucena AJG, Avezum A, Sousa ALL, Pio-Abreu A, Sposito AC, Pierin AMG, Paiva AMG, Spinelli ACS, Nogueira ADR, Dinamarco N, Eibel B, Forjaz CLM, Zanini CRO, Souza CB, Souza DDSM, Nilson EAF, Costa EFA, Freitas EV, Duarte EDR, Muxfeldt ES, Lima Júnior E, Campana EMG, Cesarino EJ, Marques F, Argenta F, Consolim-Colombo FM, Baptista FS, Almeida FA, Borelli FAO, Fuchs FD, Plavnik FL, Salles GF, Feitosa GS, Silva GVD, Guerra GM, Moreno Júnior H, Finimundi HC, Back IC, Oliveira Filho JB, Gemelli JR, Mill JG, Ribeiro JM, Lotaif LAD, Costa LSD, Magalhães LBNC, Drager LF, Martin LC, Scala LCN, Almeida MQ, Gowdak MMG, Klein MRST, Malachias MVB, Kuschnir MCC, Pinheiro ME, Borba MHE, Moreira Filho O, Passarelli Júnior O, Coelho OR, Vitorino PVO, Vitorino PVO, Ribeiro Junior RM, Esporcatte R, Franco R, Pedrosa R, Mulinari RA, Paula RB, Okawa RTP, Rosa RF, Amaral SLD, Ferreira-Filho SR, Kaiser SE, Jardim TSV, Guimarães V, Koch VH, Oigman W, Nadruz W.   +97 more
europepmc   +1 more source

Características epidemiológicas de los recién nacidos con hiperplasia suprarrenal congénita diagnosticada por tamizaje neonatal en Hospital Víctor Lazarte Echegaray. 2011 - 2015

, 2018
To determine the epidemiological characteristics of congenital adrenal hyperplasia. Method: Descriptive, retrospective, cross-sectional study of 16 positive neonates for congenital adrenal hyperplasia by neonatal screening in the Neonatal Screening ...
Zapata Chávez, Roberto Manuel
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Clinical case seminar - Hypogonadotropic hypogonadism as a presenting feature of late-onset X-linked adrenal hypoplasia congenita [PDF]

, 2002
Mutations in the orphan nuclear receptor DAX-1 cause X-linked adrenal hypoplasia congenita. Affected boys usually present with primary adrenal failure in early infancy or childhood.
Beck-Peccoz, P, Achermann, JC, Romoli, R, Spada, A, Mantovani, G, Persani, L, Jameson, JL, Ozisik, G, Borretta, G   +8 more
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Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review. [PDF]

Sao Paulo Med J, 2011
Marchini GS, Cocuzza M, Pagani R, Torricelli FC, Hallak J, Srougi M.   +5 more
europepmc   +1 more source

Brazilian Position Statement on the Use Of Multimodality Imaging in Cardio-Oncology - 2021. [PDF]

Arq Bras Cardiol, 2021
Melo MDT, Paiva MG, Santos MVC, Rochitte CE, Moreira VM, Saleh MH, Brandão SCS, Gallafrio CC, Goldwasser D, Gripp EA, Piveta RB, Silva TO, Santo THCE, Ferreira WP, Salemi VMC, Cauduro SA, Barberato SH, Lopes HMC, Pena JLB, Rached HRS, Miglioranza MH, Pinheiro AC, Vrandecic BALM, Cruz CBBV, Nomura CH, Cerbino FME, Costa IBSDS, Coelho Filho OR, Carneiro ACC, Burgos UMMC, Fernandes JL, Uellendahl M, Calado EB, Senra T, Assunção BL, Freire CMV, Martins CN, Sawamura KSS, Brito MM, Jardim MFS, Bernardes RJM, Diógenes TC, Vieira LO, Mesquita CT, Lopes RW, Segundo Neto EMV, Rigo L, Marin VLS, Santos MJ, Grossman GB, Quagliato PC, Alcantara ML, Teodoro JAR, Albricker ACL, Barros FS, Amaral SID, Porto CLL, Barros MVL, Santos SND, Cantisano AL, Petisco ACGP, Barbosa JEM, Veloso OCG, Spina S, Pignatelli R, Hajjar LA, Kalil Filho R, Lopes MACQ, Vieira MLC, Almeida ALC.   +69 more
europepmc   +1 more source

Position Statement on Ischemic Heart Disease - Women-Centered Health Care - 2023. [PDF]

Arq Bras Cardiol, 2023
Oliveira GMM, Almeida MCC, Rassi DDC, Bragança ÉOV, Moura LZ, Arrais M, Campos MDSB, Lemke VG, Avila WS, Lucena AJG, Almeida ALC, Brandão AA, Ferreira ADA, Biolo A, Macedo AVS, Falcão BAA, Polanczyk CA, Lantieri CJB, Marques-Santos C, Freire CMV, Pellegrini D, Alexandre ERG, Braga FGM, Oliveira FMF, Cintra FD, Costa IBSDS, Silva JSN, Carreira LTF, Magalhães LBNC, Matos LDNJ, Assad MHV, Barbosa MM, Silva MGD, Rivera MAM, Izar MCO, Costa MENC, Paiva MSMO, Castro ML, Uellendahl M, Oliveira Junior MT, Souza OF, Costa RAD, Coutinho RQ, Silva SCTFD, Martins SM, Brandão SCS, Buglia S, Barbosa TMJU, Nascimento TAD, Vieira T, Campagnucci VP, Chagas ACP.   +51 more
europepmc   +1 more source

Hiperplasia suprarrenal congénita: origen de trastornos del desarrollo y diferenciación sexual

, 2019
La hiperplasia suprarrenal congénita es una patología de origen genético que se desarrolla por un déficit enzimático secundario a alteraciones en la síntesis de proteínas.
Herrera Gómez, Ana
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