Clinical Characterization of Familial Isolated Pituitary Adenomas

The prevalence of pituitary adenomas

2004 • 1,247 citations

Pituitary Adenoma Predisposition Caused by Germline Mutations in the AIP Gene

2006 • 598 citations

Pituitary Disease in MEN Type 1 (MEN1): Data from the France-Belgium MEN1 Multicenter Study

2002 • 446 citations

Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex

2000 • 403 citations

Dominant Inheritance of the Complex of Myxomas, Spotty Pigmentation, and Endocrine Overactivity

1986 • 355 citations

Age‐related and gender‐related occurrence of pituitary adenomas

1994 • 280 citations

Pituitary tumors: pathophysiology, clinical manifestations and management.

2001 • 204 citations

Minireview: PRKAR1A: Normal and Abnormal Functions

2004 • 197 citations

Mutation Analysis of theMEN1Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism¹

1998 • 162 citations

Molecular Pathology of the MEN1 Gene

2004 • 161 citations

Pituitary adenomas of the multiple endocrine neoplasia type I syndrome.

1987 • 148 citations

Genetic and Histologic Studies of Somatomammotropic Pituitary Tumors in Patients with the “Complex of Spotty Skin Pigmentation, Myxomas, Endocrine Overactivity and Schwannomas” (Carney Complex)¹

2000 • 145 citations

Mutation Analysis of the MEN1 Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism

1998 • 125 citations

Pituitary tumours

1973 • 107 citations

Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases

1999 • 95 citations

Loss of Heterozygosity on Chromosome 11q13 in Two Families with Acromegaly/Gigantism Is Independent of Mutations of the Multiple Endocrine Neoplasia Type I Gene¹

1999 • 88 citations

Predictors and rates of treatment-resistant tumor growth in acromegaly

2005 • 86 citations

Human tumors associated with Carney complex and germline PRKAR1A mutations: a protein kinase A disease!

2003 • 86 citations

Hereditary Hormone Excess: Genes, Molecular Pathways, and Syndromes

2005 • 84 citations

Pituitary tumours

2001 • 68 citations

Familial acromegaly: case report and review of the literature.

1999 • 60 citations

Tumor Deletion Mapping on Chromosome 11q13 in Eight Families with Isolated Familial Somatotropinoma and in 15 Sporadic Somatotropinomas

2005 • 53 citations

Gender-related differences in prolactinomas. A clinicopathological study.

2005 • 50 citations

Loss of Heterozygosity on Chromosome 11q13 in Two Families with Acromegaly/Gigantism Is Independent of Mutations of the Multiple Endocrine Neoplasia Type I Gene

1999 • 49 citations

A meiotic recombination in a new isolated familial somatotropinoma kindred

2004 • 44 citations

Familial prolactinoma

1995 • 42 citations

Isolated Familial Somatotropinoma

2004 • 39 citations

Clinical and Genetic Features of Familial Pituitary Adenomas

2005 • 38 citations

Malignant Prolactinoma Discovered by D2 Receptor Imaging

2000 • 33 citations

Familial acromegaly

2004 • 29 citations

Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly

2007 • 29 citations

Isolated familial somatotropinomas: clinical features and analysis of the MEN1 gene.

2002 • 29 citations

Two familial giant pituitary adenomas associated with overweight: clinical, morphological and genetic features

2001 • 18 citations

[Familial acromegaly. Apropos of a case. Review of the literature].

1992 • 16 citations

Growth hormone-, alpha-subunit and thyrotrophin-cosecreting pituitary adenoma in familial setting of pituitary tumour

1993 • 13 citations

Case Report: Cushing’s Disease in Two Sisters

1989 • 5 citations