N. Setian

发表

Adrenocortical Carcinoma: Prognostic Indices Based on Clinical and Immunohistochemical Markers

V. Dichtchekenian, C. de Bragança Pereira, H. Kuperman, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Subcutaneous use of a fast-acting insulin analog: an alternative treatment for pediatric patients with diabetic ketoacidosis.

H. Kuperman, D. Damiani, N. Setian, 2005, Diabetes care.

Macrosomia, obesity, macrocephaly and ocular abnormalities (MOMO syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndrome.

N. Setian, D. Moretti-Ferreira, C. Koiffmann, 1993, American journal of medical genetics.

[Genetic and metabolic description of five patients with Berardinelli-Seip syndrome].

C. Kim, D. Damiani, N. Setian, 2011, Arquivos brasileiros de endocrinologia e metabologia.

Proliferating Cell Nuclear Antigen Immunoreaction in Adrenal Tumors

V. Dichtchekenian, D. Damiani, V. Alves, 1995, Tumori.

Prader-Willi syndrome: genetic tests and clinical findings.

N. Setian, M. Varela, C. Koiffmann, 2000, Genetic testing.

Persistent hyperinsulinemic hypoglycemia of infancy : case report

V. Dichtchekenian, D. Damiani, N. Setian, 2022 .

Severe hypercalcemia in a 9-year-old Brazilian girl due to a novel inactivating mutation of the calcium-sensing receptor.

D. Damiani, N. Setian, I. Kunii, 2004, The Journal of clinical endocrinology and metabolism.

[Childhood hypoglycemia - still a challenge].

V. Dichtchekenian, D. Damiani, N. Setian, 1997, Jornal de pediatria.

[Search of prostatic tissue in 46,XX congenital adrenal hyperplasia].

H. Kuperman, D. Damiani, N. Setian, 2009, Arquivos brasileiros de endocrinologia e metabologia.

DNA synthesis stimulatory activity is low in serum of protein-undernourished children.

N. Setian, H. Armelin, R. Fukui, 1984, The Journal of pediatrics.

Impact of molecular mechanisms, including deletion size, on Prader–Willi syndrome phenotype: study of 75 patients

N. Setian, M. Varela, C. Koiffmann, 2004, Clinical Genetics.

Premature thelarche: identification of clinical and laboratory data for the diagnosis of precocious puberty.

V. Dichtchekenian, H. Kuperman, D. Damiani, 2002, Revista do Hospital das Clinicas.

Novel mutation in MCT8 gene in a Brazilian boy with thyroid hormone resistance and severe neurologic abnormalities.

V. Dichtchekenian, H. Kuperman, D. Damiani, 2011, Arquivos brasileiros de endocrinologia e metabologia.

Identification and functional analysis of a novel inactivating mutation (A804D) of the calcium‐sensing receptor gene

D. Damiani, N. Setian, T. Kasamatsu, 2004, Clinical endocrinology.

[Evaluation of the main late endocrine effects in children and adolescents after treatment of malignancies].

H. Kuperman, D. Damiani, N. Setian, 2010, Arquivos brasileiros de endocrinologia e metabologia.

True hermaphroditism: clinical aspects and molecular studies in 16 cases.

V. Dichtchekenian, D. Damiani, N. Setian, 1997, European journal of endocrinology.

Ullrich-Turner Syndrome: Relevance of Searching for Y Chromosome Fragments

V. Dichtchekenian, T. Manna, D. Damiani, 1999, Journal of pediatric endocrinology & metabolism : JPEM.

[True hermaphroditism: experience with 36 patients].

D. Damiani, N. Setian, G. Guerra‐Júnior, 2005, Arquivos brasileiros de endocrinologia e metabologia.

Inhibin A Production after Gonadotropin Stimulus: A New Method to Detect Ovarian Tissue in Ovotesticular Disorder of Sex Development

V. Dichtchekenian, D. Damiani, N. Setian, 2009, Hormone Research in Paediatrics.

CYP21 mutations in Brazilian patients with 21-hydroxylase deficiency

V. Dichtchekenian, D. Damiani, N. Setian, 2000, Human Genetics.

Hypothyroidism in children: diagnosis and treatment.

N. Setian, Nuvarte Setian Setian, 2007, Jornal de pediatria.

Growth and puberty after treatment for acute lymphoblastic leukemia.

V. Dichtchekenian, H. Kuperman, D. Damiani, 2004, Revista do Hospital das Clinicas.

Central diabetes insipidus as a complication of neonatal pathology: Report of three cases

D. Damiani, N. Setian, M. E. Ceccon, 1998, Acta paediatrica Japonica : Overseas edition.

Primary Hyperparathyroidism in Children: Patient Report and Review of the Literature

V. Dichtchekenian, D. Damiani, N. Setian, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

Pituitary Macroadenoma and Cushing's Disease in Pediatric Patients: Patient Report and Review of the Literature

V. Dichtchekenian, D. Damiani, N. Setian, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

Hypopituitarism, Deficiency of Factors V and VIII and von Willebrand Factor: An Uncommon Association

V. Dichtchekenian, D. Damiani, N. Setian, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome

D. Damiani, N. Setian, M. Fellous, 1990, Human Genetics.

Evaluation of Adrenal Reserve in Children with Acute Lymphocytic Leukemia Treated with Prednisone or Dexamethasone

H. Kuperman, D. Damiani, N. Setian, 2012, Hormone Research in Paediatrics.

Evaluation of the hypothalamic-pituitary-adrenal axis in children with leukemia before and after 6 weeks of high-dose glucocorticoid therapy.

G. Chrousos, V. Dichtchekenian, H. Kuperman, 2001, The Journal of clinical endocrinology and metabolism.

[XX male: 3 case reports during childhood].

V. Dichtchekenian, D. Damiani, N. Setian, 2005, Arquivos brasileiros de endocrinologia e metabologia.

A novel DAX1/NR0B1 mutation in a patient with adrenal hypoplasia congenita and hypogonadotropic hypogonadism.

V. Dichtchekenian, H. Kuperman, D. Damiani, 2012, Arquivos brasileiros de endocrinologia e metabologia.

CLINICAL CASE SEMINAR Severe Hypercalcemia in a 9-Year-Old Brazilian Girl Due to a Novel Inactivating Mutation of the Calcium-Sensing Receptor

D. Damiani, N. Setian, I. Kunii, 2004 .

Diabetes mellitus in childhood: an emerging condition in the 21st century.

V. Dichtchekenian, H. Kuperman, D. Damiani, 2016, Revista da Associacao Medica Brasileira.

Persistence of Mtillerian Remnants in Complete Androgen Insensitivity Syndrome

V. Dichtchekenian, D. Damiani, N. Setian, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Decrease of Serum Alkaline Phosphatase after Three Cycles of Pamidronate Disodium in Children with Severe Osteogenesis Imperfecta

V. Dichtchekenian, H. Kuperman, D. Damiani, 2007, Hormone Research in Paediatrics.

[True hermaphroditism: experience with 36 patients].

D. Damiani, N. Setian, G. Guerra‐Júnior, 2005, Arquivos brasileiros de endocrinologia e metabologia.

[Brain sex: just beginning to pave the way].

D. Damiani, N. Setian, D. Damiani, 2005, Arquivos brasileiros de endocrinologia e metabologia.

[Prader-Willi syndrome: metabolic aspects related to growth hormone treatment].

H. Kuperman, D. Damiani, N. Setian, 2007, Arquivos brasileiros de endocrinologia e metabologia.