Search Results - "Hayashida, Yumi"

Association between baseline Mini-Mental State Examination score and dementia incidence in a cohort of oldest old by Hayashida, Débora Yumi, Jacinto, Alessandro Ferrari, Araújo, Lara Miguel Quirino, Almada Filho, Clineu de Mello, DI Tommaso, Ana Beatriz, Cendoroglo, Maysa Seabra

“…The Brazilian population has aged rapidly. The oldest old, defined as persons aged 80 years or older, is the fastest growing segment of the Brazilian…”
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Measures taken by public health centers in Kumamoto, Japan, during the hyperacute phase to subacute phase of the Kumamoto earthquake by Tsurugi, Yoko, Ikeda, Yoichiro, Inada, Tomohisa, Ogata, Keiko, Kiwaki, Koji, Komiya, Satoshi, Nagano, Toshiro, Hattori, Kiyoko, Hayashida, Yumi, Fuchigami, Aya

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Association between baseline Mini-Mental State Examination score and dementia incidence in a cohort of oldest old by HAYASHIDA, Débora Yumi, JACINTO, Alessandro Ferrari, ARAÚJO, Lara Miguel Quirino, ALMADA FILHO, Clineu de Mello, DI TOMMASO, Ana Beatriz, CENDOROGLO, Maysa Seabra

“…ABSTRACT Background: The Brazilian population has aged rapidly. The oldest old, defined as persons aged 80 years or older, is the fastest growing segment of…”
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Clinical characteristics associated with hepatic steatosis on ultrasonography in patients with elevated alanine aminotransferase by Narciso-Schiavon, Janaína Luz, Schiavon, Leonardo de Lucca, Carvalho-Filho, Roberto José de, Hayashida, Débora Yumi, Wang, Jenny Hue Jiuan, Souza, Tatiana Santana, Emori, Christini Takemi, Ferraz, Maria Lucia Gomes, Silva, Antonio Eduardo Benedito

“…The main causes of hepatic steatosis (HS) are alcoholic liver disease and nonalcoholic fatty liver disease (NAFLD). Although liver biopsy is the gold standard…”
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Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain alpha-keto acid dehydrogenase complex by Tsuruta, M, Mitsubuchi, H, Mardy, S, Miura, Y, Hayashida, Y, Kinugasa, A, Ishitsu, T, Matsuda, I, Indo, Y

“…The E2 gene of the branched-chain alpha-keto acid dehydrogenase (BCKDH) complex was studied at the molecular level in three patients with intermittent maple…”
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Mutations in the TRKA /NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis by Indo, Yasuhiro, Tsuruta, Motoko, Hayashida, Yumi, Karim, Mohammad Azharul, Ohta, Kohji, Kawano, Tomoyasu, Mitsubuchi, Hiroshi, Tonoki, Hidefumi, Awaya, Yutaka, Matsuda, Ichiro

“…Congenital insensitivity to pain with anhidrosis (CIPA; MIM 256800) is an autosomal-recessive disorder characterized by recurrent episodes of unexplained…”
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Insights into Antimicrobial Peptides from Limacus flavus Mucus by Hayashida, Patricia Yumi, da Silva Junior, Pedro Ismael

“…Antimicrobial peptides have been a major research subject since the rise of antimicrobial resistance as a major public health problem. These molecules are…”
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Lonomia obliqua’s hemolymph: new horizons to antibiotics by Hayashida, Patricia Yumi, Da Silva Junior, Pedro Ismael, Mendonça, Ronaldo Zucatelli

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Duffy-negative is associated with hemolytic phenotype of sickle cell anemia. Authors' reply by MECABO, Grazielle, YUMI HAYASHIDA, Debora, MUKISI-MUKAZA, Martin, ELION, Jacques, ROMANA, M, HARDY-DESSOURCES, Marie-Dominique, AZEVEDO-SHIMMOTO, Marily Maria, VICARI, Perla, DE ALMEIDA SANTOS ARRUDA, Martha Mariana, BORDIN, José Orlando, FIGUEIREDO, Maria Stella, NEBOR, Danitza, DURPES, Marie Claude, MOUGENEL, Danielle

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Duffy-negative is associated with hemolytic phenotype of sickle cell anemia by Mecabo, Grazielle, Hayashida, Debora Yumi, Azevedo-Shimmoto, Marily Maria, Vicari, Perla, Arruda, Martha Mariana de Almeida Santos, Bordin, José Orlando, Figueiredo, Maria Stella

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Heterogeneity of mutations in maple syrup urine disease (MSUD): screening and identification of affected E1 alpha and E1 beta subunits of the branched-chain alpha-keto-acid dehydrogenase multienzyme complex by Nobukuni, Y, Mitsubuchi, H, Hayashida, Y, Ohta, K, Indo, Y, Ichiba, Y, Endo, F, Matsuda, I

“…Maple syrup urine disease (MSUD) is an autosomal recessive disease caused by a deficiency in subunits of the branched-chain alpha-keto-acid dehydrogenase…”
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