L. Calliari

发表

Thyroid Carcinoma During Childhood and Adolescence

C. Longui, C. Kochi, N. Scalissi, 2005 .

Metabolic Syndrome in Adolescents with Type 1 Diabetes Mellitus in a Mixed Population: Are Girls at a Higher Risk?

L. Calliari, T. Homma, R. M. Noronha, 2017 .

Clinical experience with radioactive iodine in the treatment of childhood and adolescent Graves' disease

C. Longui, C. Kochi, N. Scalissi, 2012, Endocrine connections.

[Radioactive iodine therapy for Graves' disease in childhood and adolescence].

C. Longui, O. Monte, L. Calliari, 2004, Arquivos brasileiros de endocrinologia e metabologia.

Thyroid function and autoimmunity in children and adolescents with Type 1 Diabetes Mellitus.

L. Calliari, Aline Dantas Costa Riquetto, Renata Maria de Noronha, 2015, Diabetes research and clinical practice.

Dyslipidemia in young patients with type 1 diabetes mellitus.

O. Monte, L. Calliari, T. Homma, 2015, Archives of endocrinology and metabolism.

Infections in children with diabetes

F. J. Almeida, L. Calliari, R. M. Noronha, 2019, Jornal de Pediatria.

Mild adrenal insufficiency due to a NROB1 (DAX1) gene mutation in a boy presenting an association of hypogonadotropic hypogonadism, reduced final height and attention deficit disorder.

C. Longui, O. Monte, M. Rocha, 2013, Arquivos brasileiros de endocrinologia e metabologia.

A novel mutation in DAX1 gene causing different phenotypes in three siblings with adrenal hypoplasia congenita.

C. Longui, C. Kochi, O. Monte, 2007, Genetics and molecular research : GMR.

[Comparative study of prednisolone versus hydrocortisone acetate for treatment of patients with the classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency].

C. Longui, C. Kochi, O. Monte, 2008, Arquivos brasileiros de endocrinologia e metabologia.

Partial Glucocorticoid Resistance in Obese Children Detected by Very Low Dose Dexamethasone Suppression Test

C. Longui, C. Kochi, O. Monte, 2003, Journal of pediatric endocrinology & metabolism : JPEM.

Importance of screening with oral glucose tolerance test for early diagnosis of cystic fibrosis‐related diabetes mellitus

O. Monte, L. Calliari, R. M. Noronha, 2014, Pediatric diabetes.

Update on diagnosis and monitoring of cystic fibrosis-related diabetes mellitus (CFRD).

O. Monte, L. Calliari, R. M. Noronha, 2011, Arquivos brasileiros de endocrinologia e metabologia.

[Growth hormone therapy and hypersensitivity type III reaction: a contraindication for desensitization].

C. Longui, C. Kochi, O. Monte, 2011, Arquivos brasileiros de endocrinologia e metabologia.

Evaluation of AC(n) and C(-106)T polymorphisms of the aldose reductase gene in Brazilian patients with DM1 and susceptibility to diabetic retinopathy

C. Longui, M. Barbosa de Melo, O. Monte, 2007, Molecular vision.

Near-final height in patients with congenital adrenal hyperplasia treated with combined therapy using GH and GnRHa.

C. Longui, C. Kochi, O. Monte, 2011, Arquivos brasileiros de endocrinologia e metabologia.

Inhibin α-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers

C. Stratakis, G. Guerra‐Júnior, A. Moreira, 2004, Journal of Medical Genetics.

Fast Acquisition Sagittal TI Magnetic Resonance Imaging (FAST1-MRI): A New Imaging Approach for the Diagnosis of Growth Hormone Deficiency

Cristiane Kochi, C. Longui, C. Kochi, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome.

G. Guerra‐Júnior, C. Longui, C. Kochi, 2007, Genetics and molecular research : GMR.

Size of the exon 1-CAG repeats of the androgen receptor gene employed as a molecular marker in the diagnosis of Turner syndrome in girls with short stature.

C. Longui, C. Kochi, O. Monte, 2008, Genetics and molecular research : GMR.