Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Liliana Mitie Suganuma"'
1
Heterogeneous phenotype of Hereditary Xerocytosis in association with PIEZO1 variants
Autor: Murilo Castro Cervato, Roberta Sitnik, Sandra Fátima Menosi Gualandro, João Renato Rebello Pinho, Narla Mohandas, Paulo Augusto Achucarro Silveira, Nair Hideko Muto, Liliana Mitie Suganuma, Andrea Balan, Guilherme Henrique Hencklain Fonseca, Priscila de Meira Oliveira
Publikováno v: Blood cells, moleculesdiseases. 82
Hereditary Xerocytosis (HX) is an autosomal dominantly inherited congenital hemolytic anemia associated with erythrocyte dehydration due to decreased intracellular potassium content resulting in increased mean corpuscular hemoglobin concentration. Th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fe9ca9455f52350c6185bbfa375276f
https://pubmed.ncbi.nlm.nih.gov/32109669
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2
Temporomandibular joint arthritis in sickle cell disease: a case report
Autor: Guilherme Henrique Hencklain Fonseca, José Tadeu Tesseroli de Siqueira, Levi H. Jales Neto, Sandra Fátima Menosi Gualandro, Maíra da Silva Caracas, Joice Carla da Silva Castro, Liliana Mitie Suganuma, Sumatra Jales
Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
We report a rare case of aseptic arthritis in the temporomandibular joint of a patient with sickle cell anemia. A 22-year-old woman with sickle cell disease, in the 18th week of gestation, was referred by her hematologist to investigate a sudden mout
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9faec0537c6c10833fd5bf07c579fd3e
https://doi.org/10.1016/j.oooo.2012.05.018
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3
Porfirias: quadro clínico, diagnóstico e tratamento
Autor: Sandra Fátima Menosi Gualandro, Dalton de Alencar Fischer Chamone, Carla Luana Dinardo, Guilherme Henrique Hencklain Fonseca, Liliana Mitie Suganuma
Publikováno v: Revista de Medicina. 89:106-114
As porfirias são doenças incomuns e de herança genética na maior parte dos casos. As porfirias são divididas em eritropoiéticas, hepáticas agudas e hepáticas crônicas. Os subtipos de maior relevância clínica são a porfiria cutânea tarda
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::da2e039c27e090d36e42dcfdb9fb5e5e
https://doi.org/10.11606/issn.1679-9836.v89i2p106-114
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4
Talidomida no tratamento de angiodisplasias intestinais em paciente com síndrome CREST - relato de caso e revisão da literatura
Autor: Carla Luana Dinardo, Sandra Fátima Menosi Gualandro, Liliana Mitie Suganuma, Guilherme Henrique Hencklain Fonseca, Paulo Sérgio Panse Silveira
Publikováno v: Revista de Medicina. 88:103-106
A anemia ferropriva grave secundária à hemorragia digestiva por angiodisplasiasintestinais representa um grande desafio terapêutico. Comumente, as ectasias vasculares sãomúltiplas e dispersas ao longo do intestino, limitando a eficácia do trata
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0a189729377e1dbd18a7173f32821640
https://doi.org/10.11606/issn.1679-9836.v88i2p103-106
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5
Cohort study of adult patients with haemoglobin SC disease: clinical characteristics and predictors of mortality
Autor: Danielle Menosi Gualandro, Iara K. Yokomizo, Sandra F. Mm Gualandro, Liliana Mitie Suganuma, Guilherme Henrique Hencklain Fonseca
Publikováno v: British journal of haematology. 171(4)
Haemoglobin (Hb) SC disease is the second most common subtype of sickle cell disease and is potentially fatal. This study aimed to determine the clinical characteristics, outcome and predictors of mortality in HbSC disease patients, and to compare th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23cd43b25a49b8882301dd25f3ac4128
https://pubmed.ncbi.nlm.nih.gov/26255986
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6
Tuberculosis in hematopoietic stem cell transplant patients: case report and review of the literature
Autor: Rachel Russo, Silvia Figueiredo Costa, Liliana Mitie Suganuma, Maria Aparecida Shikanai Yasuda, Ivan França, Frederico Luiz Dulley
Publikováno v: International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases. 14
The literature describing tuberculosis (TB) in hematopoietic stem cell transplant (HSCT) recipients is scant, even in countries where TB is common. We describe a case of pulmonary TB in a patient who underwent HSCT and review the English language lit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50dc53c344c6b97b8ed52c156038a1fd
https://pubmed.ncbi.nlm.nih.gov/19819176
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7
Hemophilia and child abuse as possible causes of epidural hematoma: case report
Autor: Liliana Mitie Suganuma, Ricardo B. V. Fontes, Almir Ferreira de Andrade, Fernando Campos Gomes Pinto, Raul Marino, Fabrizio Frutos Porro
Publikováno v: Arquivos de Neuro-Psiquiatria v.61 n.4 2003
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
INTRODUCTION: Head trauma is an important consequence of child abuse. Specific pathophysiological mechanisms in child abuse are responsible for the ''whiplash shaken-baby syndrome'', which would favour the occurrence of intracranial hemorrhages. CASE
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::500b4b32dae985bb115463fc8a088bac
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2003000600026
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