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La ricerca find articoli where authors phrase all words 'MEDEIROSNETO G' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 29 riferimenti
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    1. TARGOVNIK HM; FRECHTEL GD; MENDIVE FM; VONO J; COCHAUX P; VASSART G; MEDEIROSNETO G
      EVIDENCE FOR THE SEGREGATION OF 3 DIFFERENT MUTATED ALLELES OF THE THYROGLOBULIN GENE IN A BRAZILIAN FAMILY WITH CONGENITAL GOITER AND HYPOTHYROIDISM

      Thyroid
    2. STANBURY JB; ERMANS AE; BOURDOUX P; TODD C; OKEN E; TONGLET R; VIDOR G; BRAVERMAN LE; MEDEIROSNETO G
      IODINE-INDUCED HYPERTHYROIDISM - OCCURRENCE AND EPIDEMIOLOGY

      Thyroid
    3. CAMARGO RYA; GROSS JL; SILVEIRO SP; KNOBEL M; MEDEIROSNETO G
      PATHOLOGICAL FINDINGS IN DYSHORMONOGENETIC GOITER WITH DEFECTIVE IODIDE TRANSPORT

      Endocrine pathology
    4. MEDEIROSNETO G; GILDACOSTA MJ; SANTOS CLS; MEDINA AM; SILVA JCE; TSOU RM; SOBRINHOSIMOES M
      METASTATIC THYROID-CARCINOMA ARISING FROM CONGENITAL GOITER DUE TO MUTATION IN THE THYROPEROXIDASE GENE

      The Journal of clinical endocrinology and metabolism
    5. LIMA N; KNOBEL M; CAVALIERE H; SZTEJNSZNAJD C; TOMIMORI E; MEDEIROSNETO G
      LEVOTHYROXINE SUPPRESSIVE THERAPY IS PARTIALLY EFFECTIVE IN TREATING PATIENTS WITH BENIGN, SOLID THYROID-NODULES AND MULTINODULAR GOITERS

      Thyroid
    6. REGO KGM; BILLERBECK AEC; TARGOVNIK HM; SANTOS CLS; ALKMIN MG; BARBOSA S; CAMARGO R; MEDEIROSNETO G
      CLINICAL, PATHOLOGICAL, AND MOLECULAR STUDIES OF 2 FAMILIES WITH IODIDE ORGANIFICATION DEFECT

      Endocrine pathology
    7. MEDEIROSNETO G; DELACERDA L; WONDISFORD FE
      FAMILIAL CONGENITAL HYPOTHYROIDISM CAUSED BY ABNORMAL AND BIOINACTIVETSH DUE TO MUTATIONS IN THE BETA-SUBUNIT GENE

      Trends in endocrinology and metabolism
    8. MEDEIROSNETO G; BUNDUKI V; TOMIMORI E; GOMES S; KNOBEL M; MARTIN RT; ZUGAIB M
      PRENATAL-DIAGNOSIS AND TREATMENT OF DYSHORMONOGENETIC FETAL GOITER DUE TO DEFECTIVE THYROGLOBULIN SYNTHESIS

      The Journal of clinical endocrinology and metabolism
    9. POHLENZ J; MEDEIROSNETO G; GROSS JL; SILVEIRO SP; KNOBEL M; REFETOFF S
      HYPOTHYROIDISM IN A BRAZILIAN KINDRED DUE TO IODIDE TRAPPING DEFECT CAUSED BY A HOMOZYGOUS MUTATION IN THE SODIUM IODIDE SYMPORTER GENE/

      Biochemical and biophysical research communications
    10. PEDRINOLA F; SZTEJNSZNAJD C; LIMA N; HALPERN A; MEDEIROSNETO G
      THE ADDITION OF DEXFENFLURAMINE TO FLUOXETINE IN THE TREATMENT OF OBESITY - A RANDOMIZED CLINICAL-TRIAL

      Obesity research
    11. MEDEIROSNETO G; SAWIN CT
      FREIREALLEMAO,FRANCISCO (1797-1874) AND THE EARLY STUDY OF ENDEMIC GOITER IN BRAZIL

      The Endocrinologist
    12. VONO J; LIMA N; KNOBEL M; MEDEIROSNETO G
      THE EFFECT OF ORAL-ADMINISTRATION OF IODINE TO PATIENTS WITH GOITER AND HYPOTHYROIDISM DUE TO DEFECTIVE SYNTHESIS OF THYROGLOBULIN

      Thyroid
    13. BAGGIO MC; MEDEIROSNETO G; OSAWA Y; NGUYEN NY; SANTISTEBAN P; KNOBEL M; GROLLMAN EF
      AMINO-ACID-COMPOSITION OF PROTEINS EXTRACTED FROM ENDEMIC GOITER GLANDS

      Endocrine pathology
    14. MEDEIROSNETO G
      DEXFENFLURAMINE EFFECT ON ACTH AND GH IN OBESE SUBJECTS

      Journal of endocrinological investigation
    15. MEDEIROSNETO G; KIM PS; YOO SE; VONO J; TARGOVNIK HM; CAMARGO R; HOSSAIN SA; ARVAN P
      CONGENITAL HYPOTHYROID GOITER WITH DEFICIENT THYROGLOBULIN - IDENTIFICATION OF AN ENDOPLASMIC-RETICULUM STORAGE DISEASE WITH INDUCTION OF MOLECULAR CHAPERONES

      The Journal of clinical investigation
    16. MEDEIROSNETO G; HERODOTOU DT; RAJAN S; KOMMAREDDI S; DELACERDA L; SANDRINI R; BOGUSZEWSKI MCS; HOLLENBERG AN; RADOVICK S; WONDISFORD FE
      A CIRCULATING, BIOLOGICALLY INACTIVE THYROTROPIN CAUSED BY A MUTATIONIN THE BETA-SUBUNIT GENE

      The Journal of clinical investigation
    17. SPAMBALG D; SHARIFI N; ELISEI R; GROSS JL; MEDEIROSNETO G; FAGIN JA
      STRUCTURAL STUDIES OF THE THYROTROPIN RECEPTOR AND G(S)ALPHA IN HUMANTHYROID CANCERS - LOW-PREVALENCE OF MUTATIONS PREDICTS INFREQUENT INVOLVEMENT IN MALIGNANT TRANSFORMATION

      The Journal of clinical endocrinology and metabolism
    18. GUIMARAES VC; QUINTANS J; FISFALEN ME; STRAUS FH; FIELDS PE; MEDEIROSNETO G; DEGROOT LJ
      IMMUNOSUPPRESSION OF THYROIDITIS

      Endocrinology
    19. TOMIMORI E; PEDRINOLA F; CAVALIERE H; KNOBEL M; MEDEIROSNETO G
      PREVALENCE OF INCIDENTAL THYROID-DISEASE IN A RELATIVELY LOW IODINE INTAKE AREA

      Thyroid
    20. TARGOVNIK HM; VONO J; BILLERBECK AEC; CERRONE GE; VARELA V; MENDIVE F; WAJCHENBERG BL; MEDEIROSNETO G
      A 138-NUCLEOTIDE DELETION IN THE THYROGLOBULIN RIBONUCLEIC-ACID MESSENGER IN A CONGENITAL GOITER WITH DEFECTIVE THYROGLOBULIN SYNTHESIS

      The Journal of clinical endocrinology and metabolism
    21. BILLERBECK AEC; CAVALIERE H; GOLDBERG AC; KALIL J; MEDEIROSNETO G
      CLINICAL AND MOLECULAR-GENETICS STUDIES IN PENDREDS-SYNDROME

      Thyroid
    22. MATOS PS; BISI H; MEDEIROSNETO G
      DYSHORMONOGENETIC GOITER - A MORPHOLOGICAL AND IMMUNOHISTOCHEMICAL STUDY

      Endocrine pathology
    23. MEDEIROSNETO G; CAVALIERE H; KNOBEL M; SCHEINBERG MA; LIBERMAN B; NICOLAU W; BRONSTEIN M; WAJCHENBERG BL
      THYROID AUTOANTIBODIES AND SOLUBLE INTERLEUKIN-2 RECEPTOR LEVELS IN PATIENTS WITH ACTIVE AND INACTIVE ACROMEGALY

      Endocrine journal
    24. GAITAN E; COOKSEY RC; LEGAN J; LINDSAY RH; INGBAR SH; MEDEIROSNETO G
      ANTITHYROID EFFECTS IN-VIVO AND IN-VITRO OF BABASSU AND MANDIOCA - A STAPLE FOOD IN GOITER AREAS OF BRAZIL

      European journal of endocrinology
    25. KNOBEL M; BARCA MF; PEDRINOLA F; MEDEIROSNETO G
      PREVALENCE OF ANTITHYROID PEROXIDASE ANTIBODIES IN AUTOIMMUNE AND NONAUTOIMMUNE THYROID-DISORDERS IN A RELATIVELY LOW-IODINE ENVIRONMENT

      Journal of endocrinological investigation
    26. MEDEIROSNETO G
      UNTITLED

      Clinical endocrinology
    27. MEDEIROSNETO G; LIMA N; PEROZIM L; PEDRINOLA F; WAJCHENBERG BL
      THE EFFECT OF HYPOCALORIC DIET WITH AND WITHOUT D-FENFLURAMINE TREATMENT ON GROWTH-HORMONE RELEASE AFTER GROWTH HORMONE-RELEASING FACTOR STIMULATION IN PATIENTS WITH ANDROID OBESITY

      Metabolism, clinical and experimental
    28. KNOBEL M; BISI H; PERES CD; MEDEIROSNETO G
      STUDIES ON FUNCTIONAL AND MORPHOLOGICAL ASPECTS IN HUMAN MULTINODULARSIMPLE GOITER TISSUES

      Endocrine pathology
    29. TARGOVNIK HM; MEDEIROSNETO G; VARELA V; COCHAUX P; WAJCHENBERG BL; VASSART G
      A NONSENSE MUTATION CAUSES HUMAN HEREDITARY CONGENITAL GOITER WITH PREFERENTIAL PRODUCTION OF A 171-NUCLEOTIDE-DELETED THYROGLOBULIN RIBONUCLEIC-ACID MESSENGER

      The Journal of clinical endocrinology and metabolism


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/10/20 alle ore 11:58:48