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N. Setian · SciRah

Researcher profile · Semantic Scholar

N. Setian

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N. Setian — researcher profile on SciRah

h-index: 14
Works: 57
Citations: 816

Most-cited papers

Impact of molecular mechanisms, including deletion size, on Prader–Willi syndrome phenotype: study of 75 patients
M. Varela, F. Kok, N. Setian, C. A. Kim +1 more
2004Clinical Genetics117 citations
Semantic Scholar
Subcutaneous use of a fast-acting insulin analog: an alternative treatment for pediatric patients with diabetic ketoacidosis.
T. Della Manna, L. Steinmetz, P. R. Campos, S. Farhat +4 more
2005Diabetes Care115 citations Open access
Semantic Scholar
Hypothyroidism in children: diagnosis and treatment.
N. Setian
2007Jornal de Pediatria89 citations
Semantic Scholar
True hermaphroditism: clinical aspects and molecular studies in 16 cases.
Durval Damiani, M. Fellous, K. McElreavey, S. Barbaux +3 more
1997European Journal of Endocrinology77 citations
Semantic Scholar
Evaluation of the hypothalamic-pituitary-adrenal axis in children with leukemia before and after 6 weeks of high-dose glucocorticoid therapy.
H. Kuperman, Durval Damiani, G. Chrousos, V. Dichtchekenian +3 more
2001Journal of Clinical Endocrinology and Metabolism57 citations
Semantic Scholar
Prader-Willi Syndrome: Genetic Tests and Clinical Findings
C. Fridman, M. Varela, F. Kok, N. Setian +1 more
2000Genetic Testing29 citations
Semantic Scholar
Severe hypercalcemia in a 9-year-old Brazilian girl due to a novel inactivating mutation of the calcium-sensing receptor.
K. Miyashiro, I. Kunii, T. Della Manna, H. C. de Menezes +3 more
2004Journal of Clinical Endocrinology and Metabolism28 citations Open access
Semantic Scholar
Primary Hyperparathyroidism in Children: Patient Report and Review of the Literature
Durval Damiani, C. Aguiar, Viridiana S. Bueno, F. Montenegro +5 more
1998Journal of Pediatric Endocrinology & Metabolism (JPEM)27 citations
Semantic Scholar
Novel mutation in MCT8 gene in a Brazilian boy with thyroid hormone resistance and severe neurologic abnormalities.
H. C. de Menezes, S. Marui, T. Della Manna, E. Brust +5 more
2011Arquivos brasileiros de endocrinologia e metabologia21 citations Open access
Semantic Scholar
Precocious Puberty: An Endocrine Manifestation in Congenital Toxoplasmosis
N. Setian, R. S. Andrade, H. Kuperman, T. Della Manna +2 more
2002Journal of Pediatric Endocrinology & Metabolism (JPEM)18 citations
Semantic Scholar
Persistence of Mtillerian Remnants in Complete Androgen Insensitivity Syndrome
Durval Damiani, M. A. Mascolli, Michael Almeida, F. Jaubert +5 more
2002Journal of Pediatric Endocrinology & Metabolism (JPEM)17 citations
Semantic Scholar
[True hermaphroditism: experience with 36 patients].
Durval Damiani, D. R. Guedes, D. Damiani, N. Setian +3 more
2005Arquivos brasileiros de endocrinologia e metabologia16 citations Open access
Semantic Scholar
Premature thelarche: identification of clinical and laboratory data for the diagnosis of precocious puberty.
T. Della Manna, N. Setian, D. Damiani, H. Kuperman +1 more
2002Revista do Hospital das Clínicas15 citations Open access
Semantic Scholar
Rathke's cleft cyst as a cause of growth hormone deficiency and micropenis
N. Setian, C. Aguiar, J. A. Galvão, C. Crivellaro +2 more
1999Child's Nervous System15 citations
Semantic Scholar
Inhibin A Production after Gonadotropin Stimulus: A New Method to Detect Ovarian Tissue in Ovotesticular Disorder of Sex Development
L. Steinmetz, M. N. Rocha, C. Longui, D. Damiani +2 more
2009Hormone Research in Paediatrics14 citations
Semantic Scholar
Hypopituitarism, Deficiency of Factors V and VIII and von Willebrand Factor: An Uncommon Association
N. Setian, C. M. Tanaka, D. Damiani, V. Dichtchekenian +2 more
2002Journal of Pediatric Endocrinology & Metabolism (JPEM)14 citations
Semantic Scholar
CYP21 mutations in Brazilian patients with 21-hydroxylase deficiency
S. Witchel, Rhonda R. Smith, C. Crivellaro, T. Della Manna +3 more
2000Human Genetics14 citations
Semantic Scholar
Growth and puberty after treatment for acute lymphoblastic leukemia.
Claudia Helena Bastos da Silva Alves, H. Kuperman, V. Dichtchekenian, D. Damiani +4 more
2004Revista do Hospital das Clínicas13 citations Open access
Semantic Scholar
A novel DAX1/NR0B1 mutation in a patient with adrenal hypoplasia congenita and hypogonadotropic hypogonadism.
Claudilene Battistin, H. C. de Menezes, S. Domenice, M. Nishi +6 more
2012Arquivos brasileiros de endocrinologia e metabologia12 citations Open access
Semantic Scholar
Evaluation of Adrenal Reserve in Children with Acute Lymphocytic Leukemia Treated with Prednisone or Dexamethasone
H. Kuperman, V. Odone, L. Cristófani, Maria Tereza Assis de Almeida +2 more
2012Hormone Research in Paediatrics12 citations
Semantic Scholar
Diabetes mellitus in childhood: an emerging condition in the 21st century.
T. Della Manna, N. Setian, R. Savoldelli, D. R. Guedes +6 more
2016Revista da Associação Médica Brasileira11 citations Open access
Semantic Scholar
[Multicentric study of Brazilian patients with 21-hydroxylase deficiency: a genotype-phenotype correlation].
Tânia A. S. S. Bachega, A. E. Billerbeck, Érica B. Parente, S. Lemos-Marini +9 more
2004Arquivos brasileiros de endocrinologia e metabologia10 citations
Semantic Scholar
Central diabetes insipidus as a complication of neonatal pathology: Report of three cases
Vera Lúcia Jornada Krebs, D. Damiani, E. M. Diniz, Maria Esther Ceccon +5 more
1998Acta paediatrica Japonica : Overseas edition10 citations
Semantic Scholar
Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome
D. Damiani, A. E. Billerbeck, A. Goldberg, N. Setian +2 more
1990Human Genetics10 citations
Semantic Scholar
[Founder effect of E180splice mutation in growth hormone receptor gene (GHR) identified in Brazilian patients with GH insensitivity].
A. A. de Lima Jorge, H. C. de Menezes, Theresa S. Soares Lins, D. R. Guedes +4 more
2005Arquivos brasileiros de endocrinologia e metabologia9 citations
Semantic Scholar
[Brain sex: just beginning to pave the way].
D. Damiani, D. Damiani, T. M. Ribeiro, N. Setian
2005Arquivos brasileiros de endocrinologia e metabologia7 citations Open access
Semantic Scholar
[Thyroid carcinoma in children and adolescents - review of six cases]
Durval Damiani, V. Dichtchekenian, N. Setian, Daniela V. M. Szeliga +4 more
2001Jornal de Pediatria6 citations Open access
Semantic Scholar
[XX male: 3 case reports during childhood].
D. Damiani, D. R. Guedes, D. Damiani, V. Dichtchekenian +5 more
2005Arquivos brasileiros de endocrinologia e metabologia5 citations
Semantic Scholar
Identification and functional analysis of a novel inactivating mutation (A804D) of the calcium‐sensing receptor gene
K. Miyashiro, T. Kasamatsu, L. Steinmetz, H. C. de Menezes +3 more
2004Clinical Endocrinology5 citations
Semantic Scholar
[Search of prostatic tissue in 46,XX congenital adrenal hyperplasia].
Rose Paulino Mariana da Costa, L. Steinmetz, H. C. de Menezes, H. Kuperman +6 more
2009Arquivos brasileiros de endocrinologia e metabologia4 citations
Semantic Scholar
Adrenocortical Carcinoma: Prognostic Indices Based on Clinical and Immunohistochemical Markers
V. Dichtchekenian, C. A. de Bragança Pereira, H. Kuperman, T. D. Manna +4 more
2005Journal of Pediatric Endocrinology & Metabolism (JPEM)4 citations
Semantic Scholar
Proliferating Cell Nuclear Antigen Immunoreaction in Adrenal Tumors
D. Damiani, Tais Della Manna, Luz Graciela Wild Aquino, V. Dichtchekenian +4 more
1995Tumori4 citations
Semantic Scholar
[Genetic and metabolic description of five patients with Berardinelli-Seip syndrome].
C. B. Barra, R. Savoldelli, T. D. Manna, C. Kim +4 more
2011Arquivos brasileiros de endocrinologia e metabologia3 citations Open access
Semantic Scholar
[Prader-Willi syndrome: metabolic aspects related to growth hormone treatment].
J. Y. Kuo, Vaê Ditchekenian, T. D. Manna, H. Kuperman +2 more
2007Arquivos brasileiros de endocrinologia e metabologia2 citations
Semantic Scholar
[Persistent hyperinsulinemic hypoglycemia of infancy: case report]
Dione F. Lazarine, M. Pahl, D. Damiani, V. Dichtchekenian +2 more
2000Jornal de Pediatria2 citations Open access
Semantic Scholar
Rectal Diluted Levothyroxine for the Treatment of Neonatal Hypothyroidism: An Alternative Route of Administration
Marina Ybarra, Claudia Pinheiro, N. Setian, D. Damiani +1 more
20151 citations
Semantic Scholar
Anomalies of 46, XY Sexual Differentiation-The Role of SRY and NR5A1
D. R. Guedes, P. Pieri, R. Filippi, K. McElreavey +4 more
20131 citations
Semantic Scholar
[Evaluation of the main late endocrine effects in children and adolescents after treatment of malignancies].
H. Kuperman, Claudilene Battistin, A. Moreira, A. L. Cornacchioni +3 more
2010Arquivos brasileiros de endocrinologia e metabologia1 citations
Semantic Scholar
[Cystic fibrosis-related diabetes: a frequent co-morbidity].
T. Della Manna, N. Setian, J. Rodrigues
2008Arquivos brasileiros de endocrinologia e metabologia1 citations
Semantic Scholar
Characterization of GH secretory ability of GH deficient children: Response to MK-0677
H. Yu, Á. Arango, B. Bercu, Ma Bach +9 more
19981 citations
Semantic Scholar
Exaggerated Adrenarche and Exogenous Obesity: A Diagnostic Challenge
Marianna Ferreira, Beatriz Semmer, E. Queiroz, Nathalia Brigatti +8 more
20160 citations
Semantic Scholar
Mixed Gonadal Disgenesia: Patients of Instituto da Crianca, HC-FMUSP
Marianna Ferreira, Claudia Pinheiro, E. Queiroz, Nathalia Brigatti +8 more
20160 citations
Semantic Scholar
Increase of bone mineral density in patients with osteogenesis imperfecta treated with pamidronate disodium.
Menezes Filho Hamilton Cabral de, Brito Pupo Joyce de, Magalhaes Velasco Bastos Paula de, K. Ae +5 more
20150 citations
Semantic Scholar
Central Diabetes Insipidus Caused by Congenital Cytomegalovirus: a Rare Association?
S. Dos, C. Passone, L. Steinmetz, L. Cominato +7 more
20140 citations
Semantic Scholar
McCune-Albright Syndrome Associated to Hypophosphatemic Rickets
S. Dos, C. Passone, H. C. de Menezes, H. Kuperman +7 more
20140 citations
Semantic Scholar
Down Syndrome and Disorders of Sex Development: Only Coincidence or More?
Joyce de Brito Pupo, S. Dos, L. Steinmetz, L. Cominato +6 more
20140 citations
Semantic Scholar
Evaluation of the effects of disodium pamidronate on the serum lipid profile in pediatric patients with severe Osteogenesis Imperfecta
H. C. Menezes-Filho, V. Radonsky, G. P. Colares-Neto, H. Kuperman +4 more
20090 citations
Semantic Scholar
Hypophosphatemic rickets and osteomalacia due to a parathyroid adenoma: A case-report
H. C. Menezes-Filho, L. G. Portela, K. J. Banwart, F. Fuks +7 more
20090 citations
Semantic Scholar
Subject Index Vol. 68, Suppl. 5, 2007
W. Arlt, N. Krone, B. Spiliotis, K. Noordam +107 more
2007Hormone Research in Paediatrics0 citations Open access
Semantic Scholar
Molecular study of HSD3D2 gene in three brazilian boys with 3beta-hydroxysteroid dehydrogenase (3beta-HSD) deficiency: First description of a splice site mutation in HSD3D2 gene
C. R. Gomes, S. Marui, E. Pinto, Rose Paulino Mariana da Costa +4 more
20060 citations
Semantic Scholar

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