Výsledky vyhledávání - "Tatielly Kruk"

Akademický článek

Are pediatricians familiar with hereditary angioedema?

Autor: Herberto José Chong-Neto, M.D., Ph.D, Bárbara Padilha Aroni, M.D, Eli Mansour, M.D, Ph.D, Eliana Toledo, M.D., Ph.D, Faradiba Sarquis Serpa, M.D., Ph.D, Luisa Karla Arruda, M.D, Ph.D, Pedro Giavina-Bianchi, M.D., Ph.D, Solange Oliveira Rodrigues Valle, M.D., Ph.D, Caroline Guth de Freitas Batista de Moraes, M.T., MSc, Tatielly Kruk, M.T., MSc, Débora Carla Chong-Silva, MD, PhD, Dirceu Solé, M.D., Ph.D, Luciana Rodrigues Silva, M.D., Ph.D, Anete S. Grumach, M.D., Ph.D, Nelson Augusto Rosário Filho, M.D., Ph.D, Régis de Albuquerque Campos, M.D., Ph.D

Publikováno v: World Allergy Organization Journal, Vol 16, Iss 6, Pp 100783- (2023)

Background: Hereditary angioedema (HAE) is an autosomal dominant disease characterized by recurrent episodes of subcutaneous or mucosal edema caused by excess bradykinin. The aim of the present study was to assess the knowledge of pediatricians about

Externí odkaz: https://doaj.org/article/c6a8a53d1b3e4401aad27152faa079db

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RELAÇÃO ENTRE GENES DA VIA MONOAMINÉRGICA E MODULAÇÃO DA DOR EM PACIENTES COM FIBROMIALGIA: REVISÃO INTEGRATIVA

Autor: Rosana Gabriella Coutinho Wundervald, LUCAS MARQUES FORTUNATO, TATIELLY KRUK, JOÃO BORGIO FIORANI BORGIO, WANIA APARECIDA PARTATA

Publikováno v: Anais do I Congresso Brasileiro de Pesquisa e Educação em Saúde On-line.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::22efdb7a59868e134550213c3839793d
https://doi.org/10.51161/conpeds/15218

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RELATIONSHIP BETWEEN GENETIC POLYMORPHISM, CLINICAL MANIFESTATIONS AND PROGNOSIS IN HEREDITARY ANGIOEDEMA: SCOPE REVIEW PROTOCOL

Autor: Fortunato, Lucas Marques, Tatielly Kruk

Hereditary Angioedema (HAE) is an autosomal dominant genetic disorder (GOKMAN, 2020; KRUK, 2020). It is a rare disease and characterized by recurrent edema that can reach deep layers of the skin and other organs (GIAVINA-BIANCHI, 2017; WILKERSON, 202

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::be6b1a49f9a66a4d31554e63a0c09b48

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SLEEP DISORDERS IN WOMEN WITH PREMENOPAUAL TRANSITION FIBROMYALGIA: SCOPE REVIEW PROTOCOL

Autor: Borgio, João Guilherme Fiorani, Fortunato, Lucas Marques, Wania Aparecida Partata, Lucélia Luna Melo-Diaz, Tatielly Kruk

Objective: Sleep disturbances are common in patients with fibromyalgia. Sleep changes throughout life. Thus, the scope review presents a protocol to track evidence of sleep disturbances in women with premenopausal fibromyalgia. Methods: The protocol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::54af02b6a4957387b8734655708b5dc7

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Relationship between obesity and musculoskeletal disorders: A scope review protocol

Autor: Tatielly Kruk, Emilton Lima Júnior, Lucas Marques Fortunato

Publikováno v: Research, Society and Development; Vol. 10 No. 8; e35210816231
Research, Society and Development; Vol. 10 Núm. 8; e35210816231
Research, Society and Development; v. 10 n. 8; e35210816231
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI

Obesity is considered a public health problem and the review of the scientific literature allows the observation of several changes in the musculoskeletal system associated with this disease. The objective of this study is to describe the relationshi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c20dab7f64178f64e4aa2811bb8ff01b
https://rsdjournal.org/index.php/rsd/article/view/16231

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Relação entre obesidade e distúrbios musculoesqueléticos: revisão sistemática e metanálise

Autor: Emilton Lima Júnior, Tatielly Kruk, Lucas Marques Fortunato

Publikováno v: Research, Society and Development; Vol. 10 No. 13; e119101320212
Research, Society and Development; Vol. 10 Núm. 13; e119101320212
Research, Society and Development; v. 10 n. 13; e119101320212
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI

Introduction: Obesity is considered a public health problem and it is associated with various musculoskeletal disorders, that haven´t been reviewed systematically. Therefore, the objective of this study was to describe the relationship between these

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d33ea1eb7e295e109c29495b262896e
https://doi.org/10.33448/rsd-v10i13.20212

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Study of angiopoietin and plasminogen genes in hereditary angioedema

Autor: Tatielly Kruk, Liya Regina Mikami, Nelson Augusto Rosário Filho, Lilian Pereira Ferrari, Marina Mendonça Dias, Luisa Karla de Paula Arruda, Adriana S. Moreno, Herberto José Chong-Neto, Wagner Narciso de Campos

Publikováno v: Revista da Associação Médica Brasileira, Vol 66, Iss 4, Pp 502-506 (2020)
Revista da Associação Médica Brasileira v.66 n.4 2020
Revista da Associação Médica Brasileira
Associação Médica Brasileira (AMB)
instacron:AMB

SUMMARY OBJECTIVE To investigate the presence of the Angiopoietin 1 (ANGPT1) and Plasminogen (PLG) mutations in patients with Hereditary Angioedema (HAE) and normal C1 esterase inhibitor (C1-INH) levels, who do not harbor the F12 gene mutation. METHO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30b4b496fa9a144dbf026e1dd9ace1cd
https://pubmed.ncbi.nlm.nih.gov/32578786

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