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

Clinical genetics, 2005-01, Vol.67 (1), p.47-52

2005

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Inhibin A production after gonadotropin stimulus: a new method to detect ovarian tissue in ovotesticular disorder of sex development

Hormone research, 2009-01, Vol.71 (2), p.94-99

2009

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Hypophosphatemic rickets and osteomalacia due to a parathyroid adenoma: A case-report

Bone (New York, N.Y.), 2009-07, Vol.45, p.S90-S90

2009

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Evaluation of the effects of disodium pamidronate on the serum lipid profile in pediatric patients with severe Osteogenesis Imperfecta

Bone (New York, N.Y.), 2009-07, Vol.45, p.S85-S85

2009

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Decrease of serum alkaline phosphatase after three cycles of pamidronate disodium in children with severe osteogenesis imperfecta

Hormone research, 2007, Vol.68 Suppl 5 (5), p.207-208

2007

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Subcutaneous Use of a Fast-Acting Insulin Analog: An alternative treatment for pediatric patients with diabetic ketoacidosis

Diabetes care, 2005-08, Vol.28 (8), p.1856-1861

2005

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Persistence of Müllerian remnants in complete androgen insensitivity syndrome

Journal of pediatric endocrinology & metabolism : JPEM, 2002-11, Vol.15 (9), p.1553

2002

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Precocious puberty: an endocrine manifestation in congenital toxoplasmosis

Journal of Pediatric Endocrinology and Metabolism, 2002-11, Vol.15 (9), p.1487

2002

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Hypopituitarism, deficiency of factors V and VIII and von Willebrand factor: an uncommon association

Journal of Pediatric Endocrinology and Metabolism, 2002-03, Vol.15 (3), p.331

2002

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Pituitary macroadenoma and Cushing's disease in pediatric patients: patient report and review of the literature

Journal of Pediatric Endocrinology and Metabolism, 1998-09, Vol.11 (5), p.665

1998

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

The journal of clinical endocrinology and metabolism, 2004-12, Vol.89 (12), p.5936-5941

2004

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Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments

Journal of Pediatric Endocrinology and Metabolism, 1999-11, Vol.12 (6), p.827

1999

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Primary hyperparathyroidism in children: patient report and review of the literature

Journal of Pediatric Endocrinology and Metabolism, 1998-01, Vol.11 (1), p.83

1998

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

The journal of clinical endocrinology and metabolism, 2001-07, Vol.86 (7), p.2993-2996

2001

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

Clinical endocrinology (Oxford), 2004-12, Vol.61 (6), p.780-782

2004

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Proliferating cell nuclear antigen immunoreaction in adrenal tumors

Tumori, 1995-07, Vol.81 (4), p.273-277

1995

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Adrenocortical carcinoma: prognostic indices based on clinical and immunohistochemical markers

Journal of Pediatric Endocrinology and Metabolism, 2005-04, Vol.18 (4), p.347

2005

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True hermaphroditism: clinical aspects and molecular studies in 16 cases

European journal of endocrinology, 1997-02, Vol.136 (2), p.201-204

1997

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CYP21 mutations in Brazilian patients with 21-hydroxylase deficiency

Human genetics, 2000-04, Vol.106 (4), p.414-419

2000

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Correlation of pathologic features with clinical outcome in pediatric adrenocortical neoplasia : a study of a Brazilian population

American journal of clinical pathology, 1994-05, Vol.101 (5), p.625-629

1994

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Persistence of Mtillerian Remnants in Complete Androgen Insensitivity Syndrome

Journal of Pediatric Endocrinology and Metabolism, 2002-01, Vol.15 (9)

2002

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Rathke's cleft cyst as a cause of growth hormone deficiency and micropenis

Child's nervous system, 1999-05, Vol.15 (5), p.271-273

1999

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Persistent hyperinsulinemic hypoglycemia of infancy: case report

Jornal de pediatria, 2000-03, Vol.76 (2), p.162-8

2000

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Childhood hypoglycemia - still a challenge

Jornal de pediatria, 1997-07, Vol.73 (4)

1997

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

American journal of medical genetics, 1993-06, Vol.46 (5), p.555-558

1993

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

Inhibin A production after gonadotropin stimulus: a new method to detect ovarian tissue in ovotesticular disorder of sex development

Hypophosphatemic rickets and osteomalacia due to a parathyroid adenoma: A case-report

Evaluation of the effects of disodium pamidronate on the serum lipid profile in pediatric patients with severe Osteogenesis Imperfecta

Decrease of serum alkaline phosphatase after three cycles of pamidronate disodium in children with severe osteogenesis imperfecta

Subcutaneous Use of a Fast-Acting Insulin Analog: An alternative treatment for pediatric patients with diabetic ketoacidosis

Persistence of Müllerian remnants in complete androgen insensitivity syndrome

Precocious puberty: an endocrine manifestation in congenital toxoplasmosis

Hypopituitarism, deficiency of factors V and VIII and von Willebrand factor: an uncommon association

Pituitary macroadenoma and Cushing's disease in pediatric patients: patient report and review of the literature

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

Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments

Primary hyperparathyroidism in children: patient report and review of the literature

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

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

Proliferating cell nuclear antigen immunoreaction in adrenal tumors

Adrenocortical carcinoma: prognostic indices based on clinical and immunohistochemical markers

True hermaphroditism: clinical aspects and molecular studies in 16 cases

CYP21 mutations in Brazilian patients with 21-hydroxylase deficiency

Correlation of pathologic features with clinical outcome in pediatric adrenocortical neoplasia : a study of a Brazilian population

Persistence of Mtillerian Remnants in Complete Androgen Insensitivity Syndrome

Rathke's cleft cyst as a cause of growth hormone deficiency and micropenis

Persistent hyperinsulinemic hypoglycemia of infancy: case report

Childhood hypoglycemia - still a challenge

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

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