Hasil Pencarian - Tatiana Amorim

  • Menampilkan 1 - 14 hasil dari 14
Perbaiki Hasil
  1. 1
    IRT/IRT as a newborn cystic fibrosis screening method: optimal cutoff points for a mixed population

    IRT/IRT as a newborn cystic fibrosis screening method: optimal cutoff points for a mixed population oleh Carolina Godoy, Pedro Paulo Brito, Tatiana Amorim, Edna Lúcia Souza, Ney Boa-Sorte

    Diterbitkan 2024-08-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Hemoglobin A2 values in sickle cell disease patients quantified by high performance liquid chromatography and the influence of alpha thalassemia

    Hemoglobin A2 values in sickle cell disease patients quantified by high performance liquid chromatography and the influence of alpha thalassemia oleh Silvana Fahel da Fonseca, Tatiana Amorim, Antônio Purificação, Marilda Gonçalves, Ney Boa-Sorte

    Diterbitkan 2015-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Dried blood spot testing for the antenatal screening of HTLV, HIV, syphilis, toxoplasmosis and hepatitis B and C: prevalence, accuracy and operational aspects

    Dried blood spot testing for the antenatal screening of HTLV, HIV, syphilis, toxoplasmosis and hepatitis B and C: prevalence, accuracy and operational aspects oleh Ney Boa-Sorte, Antônio Purificação, Tatiana Amorim, Lorena Assunção, Alan Reis, Bernardo Galvão-Castro

    Diterbitkan 2014-11-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    METABOLIC CONTROL AND BODY COMPOSITION OF CHILDREN AND ADOLESCENTS WITH PHENYLKETONURIA

    METABOLIC CONTROL AND BODY COMPOSITION OF CHILDREN AND ADOLESCENTS WITH PHENYLKETONURIA oleh Zeni Drubi Nogueira, Ney Boa-Sorte, Maria Efigênia de Queiroz Leite, Maria Betânia Pereira Toralles, Tatiana Amorim

    Diterbitkan 2021-02-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    Breastfeeding and the anthropometric profile of children with sickle cell anemia receiving follow-up in a newborn screening reference service

    Breastfeeding and the anthropometric profile of children with sickle cell anemia receiving follow-up in a newborn screening reference service oleh Zeni Drubi Nogueira, Ney Boa-Sorte, Maria Efigênia de Queiroz Leite, Márcia Miyuki Kiya, Tatiana Amorim, Silvana Fahel da Fonseca

    Diterbitkan 2015-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    Five-year performance analysis of a cystic fibrosis newborn screening program in northeastern Brazil

    Five-year performance analysis of a cystic fibrosis newborn screening program in northeastern Brazil oleh Carolina Godoy, Danielle C. Paixão, Ney C.A. Boa-Sorte, Tatiana Amorim, Luiz Vicente R.F. da Silva Filho, Edna Lúcia Souza

    Diterbitkan 2023-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    Aspectos clínicos da fenilcetonúria em serviço de referência em triagem neonatal da Bahia Clinical aspects of phenylketonuria in a reference service for neonatal screening in Bahia

    Aspectos clínicos da fenilcetonúria em serviço de referência em triagem neonatal da Bahia Clinical aspects of phenylketonuria in a reference service for neonatal screening in Bahia... oleh Tatiana Amorim, Sara P.P. Gatto, Ney Boa-Sorte, Maria Efigênia Q. Leite, Maria Inês M. M. Fontes, Junaura Barretto, Angelina X. Acosta

    Diterbitkan 2005-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  8. 8
    The c.63A>G polymorphism in the NKX2.5 gene is associated with thyroid hypoplasia in children with thyroid dysgenesis

    The c.63A>G polymorphism in the NKX2.5 gene is associated with thyroid hypoplasia in children with thyroid dysgenesis oleh Taise Lima de Oliveira Cerqueira, Yanne Ramos, Giorgia Strappa, Daniel San Martin, Mariana Jesus, Jailciele Gonzaga, Paulo Ferreira, Anabel Costa, Vladimir Fernandes, Tatiana Amorim, Ana Marice Ladeia, Helton Ramos

    Diterbitkan 2015-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  9. 9
    Neonatal Screening for MPS Disorders in Latin America: A Survey of Pilot Initiatives

    Neonatal Screening for MPS Disorders in Latin America: A Survey of Pilot Initiatives oleh Francyne Kubaski, Inês Sousa, Tatiana Amorim, Danilo Pereira, Joe Trometer, Alexandre Souza, Enzo Ranieri, Giulia Polo, Alberto Burlina, Ana Carolina Brusius-Facchin, Alice Brinckmann Oliveira Netto, Shunji Tomatsu, Roberto Giugliani

    Diterbitkan 2020-11-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  10. 10
    Adherence to PKU guidelines among patients with phenylketonuria: A cross-sectional national multicenter survey-based study in Argentina, Brazil, and Mexico

    Adherence to PKU guidelines among patients with phenylketonuria: A cross-sectional national multicenter survey-based study in Argentina, Brazil, and Mexico oleh Ana Chiesa, Norma Spécola, Monique Poubel, Marcela Vela-Amieva, Elaina Jurecki, Daniel RF Vilela, Débora Mesojedovas, Giovanna Cavalcanti Carneiro, Hernán Eiroa, Keila Hayashi Nakamura, Marcela Lopes de Almeida, Roberta Brandão Cunha, Tatiana Amorim, Ida Vanessa Doederlein Schwartz

    Diterbitkan 2024-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  11. 11
    The sickle cell trait and end stage renal disease in Salvador, Brazil.

    The sickle cell trait and end stage renal disease in Salvador, Brazil. oleh Dona J Alladagbin, Paula N Fernandes, Maria B Tavares, Jean T Brito, Geraldo G S Oliveira, Luciano K Silva, Nadia A Khouri, Marilia B Oliveira, Tatiana Amorim, Cácia M Matos, Guilherme S Ribeiro, Antônio A Lopes, Marilda S Gonçalves, Washington L C Dos-Santos

    Diterbitkan 2018-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  12. 12
    Mutation screening in the genes PAX-8, NKX2-5, TSH-R, HES-1 in cohort of 63 Brazilian children with thyroid dysgenesis

    Mutation screening in the genes PAX-8, NKX2-5, TSH-R, HES-1 in cohort of 63 Brazilian children with thyroid dysgenesis oleh Taíse Lima de Oliveira Cerqueira, Yanne Rocha Ramos, Giorgia Bruna Strappa, Mariana Souza de Jesus, Jailciele Gonzaga Santos, Camila Sousa, Gildásio Carvalho, Vladimir Fernandes, Ney Boa-Sorte, Tatiana Amorim, Thiago Magalhães Silva, Ana Marice Teixeira Ladeia, Angelina Xavier Acosta, Helton Estrela Ramos

    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  13. 13
    Population medical genetics: translating science to the community

    Population medical genetics: translating science to the community oleh Roberto Giugliani, Fernanda Bender, Rowena Couto, Aline Bochernitsan, Ana Carolina Brusius-Facchin, Maira Burin, Tatiana Amorim, Angelina Xavier Acosta, Antônio Purificação, Sandra Leistner-Segal, Maria Luiza Saraiva-Pereira, Laura Bannach Jardim, Ursula Matte, Mariluce Riegel, Augusto César Cardoso-dos-Santos, Graziella Rodrigues, Marcelo Zagonel de Oliveira, Alice Tagliani-Ribeiro, Selia Heck, Vanusa Dresch, Lavínia Schuler-Faccini, Francyne Kubaski

    Diterbitkan 2019-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  14. 14
    Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity

    Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity oleh Ana Vitoria Barban Margutti, Wilson Araújo Silva, Daniel Fantozzi Garcia, Greice Andreotti de Molfetta, Adriana Aparecida Marques, Tatiana Amorim, Vânia Mesquita Gadelha Prazeres, Raquel Tavares Boy da Silva, Irene Kazue Miura, João Seda Neto, Emerson de Santana Santos, Mara Lúcia Schmitz Ferreira Santos, Charles Marques Lourenço, Tássia Tonon, Fernanda Sperb-Ludwig, Carolina Fischinger Moura de Souza, Ida Vanessa Döederlein Schwartz, José Simon Camelo

    Diterbitkan 2020-11-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: