Search Results - D'Alva, Catarina B

  • Showing 1 - 12 results of 12
Refine Results
  1. 1
    Ethmoid glomangioma and oncogenic osteomalacia: a case report

    Ethmoid glomangioma and oncogenic osteomalacia: a case report by Muniz, Camila R, Bezerra, Gabriela A. M, da Silva, Viviane C, Aguiar, Priscilla M. F, Gerson, Gunter, D'Alva, Catarina B, Nunes, André A. A

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    A single somatic activating Asp578His mutation of the luteinizing hormone receptor causes Leydig cell tumour in boys with gonadotropin-independent precocious puberty

    A single somatic activating Asp578His mutation of the luteinizing hormone receptor causes Leydig cell tumour in boys with gonadotropin-independent precocious puberty by D'Alva, Catarina B., Brito, Vinicius N., Palhares, Heloisa M. C., Carvalho, Filomena M., Arnhold, Ivo J. P., Mendonca, Berenice B., Latronico, Ana Claudia

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    A signal peptide mutation of the arginine vasopressin gene in monozygotic twins

    A signal peptide mutation of the arginine vasopressin gene in monozygotic twins by Boson, Wolfanga L., Sarubi, Juliana C., D’Alva, Catarina B., Friedman, Eitan, Faria, Daniela, De Marco, Luiz, Wajchenberg, Bernardo

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    Hipopituitarismo Associado a Hipoglicemia: Relato de 2 Casos e Revisão da Literatura

    Hipopituitarismo Associado a Hipoglicemia: Relato de 2 Casos e Revisão da Literatura by Rocha, Catarina B. D'Alva, Pereira, Maria Adelaide A.

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  5. 5
    A single somatic activating Asp578His mutation of the luteinizing hormone receptor causes Leydig cell tumour in boys with gonadotropin-independent precocious puberty

    A single somatic activating Asp578His mutation of the luteinizing hormone receptor causes Leydig cell tumour in boys with gonadotropin-independent precocious puberty by d'Alva, Catarina B, Brito, Vinicius N, Palhares, Heloisa M C, Carvalho, Filomena M, Arnhold, Ivo J P, Mendonca, Berenice B, Latronico, Ana Claudia

    Published in Clinical endocrinology
    Get full text
    Report
    Save to List
    Saved in:
  6. 6
    A signal peptide mutation of the arginine vasopressin gene in monozygotic twins

    A signal peptide mutation of the arginine vasopressin gene in monozygotic twins by Boson, Wolfanga L., Sarubi, Juliana C., D'Alva, Catarina B., Friedman, Eitan, Faria, Daniela, De Marco, Luiz, Wajchenberg, Bernardo

    Published in Clinical Endocrinology
    Get full text
    Report
    Save to List
    Saved in:
  7. 7
    Hipopituitarismo Associado a Hipoglicemia: Relato de 2 Casos e Revisão da Literatura

    Hipopituitarismo Associado a Hipoglicemia: Relato de 2 Casos e Revisão da Literatura by Rocha, Catarina B. D'Alva, Pereira, Maria Adelaide A.

    Get full text
    Article
    Save to List
    Saved in:
  8. 8
    Early Left Ventricular Systolic Dysfunction Detected by Two-Dimensional Speckle-Tracking Echocardiography in Young Patients with Congenital Generalized Lipodystrophy

    Early Left Ventricular Systolic Dysfunction Detected by Two-Dimensional Speckle-Tracking Echocardiography in Young Patients with Congenital Generalized Lipodystrophy by Liberato, Christiane Bezerra Rocha, Olegario, Natália Bitar da Cunha, Fernandes, Virginia Oliveira, Montenegro, Ana Paula Dias Rangel, Lima, Grayce Ellen da Cruz Paiva, Batista, Lívia Aline de Araújo, Martins, Lívia Vasconcelos, Penaforte-Saboia, Jaquellyne Gurgel, Liberato, Ivan Lucas Rocha, Lopes, Larissa Ferreira, d'Alva, Catarina Brasil, Furtado, Frederico Luís Braz, Lima, Ricardo Luiz De Medeiros, Nóbrega, Lucia Helena Coelho, Lima, Josivan Gomes, Montenegro Junior, Renan Magalhães

    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  9. 9
    Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age

    Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age by Coletta, Rocio R D, Jorge, Alexander A L, D' Alva, Catarina Brasil, Pinto, Emília M, Billerbeck, Ana Elisa C, Pachi, Paulo R, Longui, Carlos A, Garcia, Ricardo M, Boguszewski, Margaret, Arnhold, Ivo J P, Mendonca, Berenice B, Costa, Elaine M F

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  10. 10
    Letter re: FSH Receptor Polymorphisms and Iatrogenic Ovarian Hyperstimulation

    Letter re: FSH Receptor Polymorphisms and Iatrogenic Ovarian Hyperstimulation by d’Alva, Catarina Brasil, Serafini, Paulo, Motta, Eduardo, Latronico, Ana Claudia, Mendonca, Berenice Bilharinho

    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  11. 11
    Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocious puberty

    Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocious puberty by Latronico, Ana Claudia, Billerbeck, Ana Elisa C., Pinto, Emilia Modolo, Brazil d'Alva, Catarina, Arnhold, Ivo Jorge P., Mendonca, Berenice B.

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  12. 12
    Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocious puberty

    Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocious puberty by Latronico, Ana Claudia, Billerbeck, Ana Elisa C, Pinto, Emilia Modolo, Brazil D'Alva, Catarina, Arnhold, Ivo Jorge P, Mendonca, Berenice B

    Published in Clinical endocrinology
    Get full text
    Report
    Save to List
    Saved in:

Search Tools: