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Treatment of Adrenocorticotropin-Dependent Cushing’s Syndrome: A Consensus Statement

The journal of clinical endocrinology and metabolism, 2008-07, Vol.93 (7), p.2454-2462

2008

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Guidelines for Acromegaly Management: An Update

The journal of clinical endocrinology and metabolism, 2009-05, Vol.94 (5), p.1509-1517

2009

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Diagnosis and Complications of Cushing’s Syndrome: A Consensus Statement

The journal of clinical endocrinology and metabolism, 2003-12, Vol.88 (12), p.5593-5602

2003

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Consensus statement: medical management of acromegaly

European journal of endocrinology, 2005-12, Vol.153 (6), p.737

2005

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Guidelines for Acromegaly Management

The journal of clinical endocrinology and metabolism, 2002-09, Vol.87 (9), p.4054-4058

2002

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Surgical Management of GH-Secreting Pituitary Adenomas: An Outcome Study Using Modern Remission Criteria

The journal of clinical endocrinology and metabolism, 2001-09, Vol.86 (9), p.4072-4077

2001

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Surgical management of GH-secreting pituitary adenomas: An outcome study using modern remission criteria

The journal of clinical endocrinology and metabolism, 2001-09, Vol.86 (9), p.4072-4077

2001

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Growth Hormone Therapy in Adults and Children

The New England journal of medicine, 1999-10, Vol.341 (16), p.1206-1216

1999

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Diagnosis and treatment of acromegaly complications

Journal of endocrinological investigation, 2003-12, Vol.26 (12), p.1242-1247

2003

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Radiosurgery for Cushing's disease after failed transsphenoidal surgery

Journal of neurosurgery, 2000-11, Vol.93 (5), p.738

2000

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The Pharmacokinetic and Pharmacodynamic Characteristics of a Long-Acting Growth Hormone (GH) Preparation (Nutropin Depot) in GH-Deficient Adults

The journal of clinical endocrinology and metabolism, 2002-10, Vol.87 (10), p.4508-4514

2002

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Octreotide as primary therapy for acromegaly

The journal of clinical endocrinology and metabolism, 1998-09, Vol.83 (9), p.3034-3040

1998

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Treatment of prolactin-secreting macroadenomas with the once-weekly dopamine agonist cabergoline

The journal of clinical endocrinology and metabolism, 1996-06, Vol.81 (6), p.2338-2343

1996

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Enhanced basal and disorderly growth hormone secretion distinguish acromegalic from normal pulsatile growth hormone release

The Journal of clinical investigation, 1994-09, Vol.94 (3), p.1277-1288

1994

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The antiviral compound enviroxime targets the 3A coding region of rhinovirus and poliovirus

Journal of Virology, 1995-07, Vol.69 (7), p.4189-4197

1995

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Poliovirus 2C region functions during encapsidation of viral RNA

Journal of Virology, 1997-11, Vol.71 (11), p.8759-8765

1997

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Radiosurgery for Pituitary Tumors and Craniopharyngiomas

Neurosurgery clinics of North America, 1999-04, Vol.10 (2), p.327-336

1999

Volltextzugriff (PDF)

Hypopituitarism

The New England journal of medicine, 1994-06, Vol.330 (23), p.1651-1662

Vance, Mary Lee

1994

Volltextzugriff (PDF)

Temporal structure of in vivo growth hormone secretory events in humans

American journal of physiology: endocrinology and metabolism, 1991-01, Vol.260 (1), p.E101-E110

1991

Volltextzugriff (PDF)

Cushing's disease resulting from pituitary corticotrophic microadenoma: Treatment results from transsphenoidal microsurgery and gamma knife radiosurgery

Neuro-chirurgie, 2002-05, Vol.48 (2-3), p.294-299

2002

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Sequence determinants of 3A-mediated resistance to enviroxime in rhinoviruses and enteroviruses

Journal of Virology, 1996-07, Vol.70 (7), p.4854-4857

1996

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Evidence that enviroxime targets multiple components of the rhinovirus 14 replication complex

Archives of virology, 1999-01, Vol.144 (8), p.1569-1585

1999

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Synthesis, Antiviral Activity, and Biological Properties of Vinylacetylene Analogs of Enviroxime

Journal of medicinal chemistry, 1997-05, Vol.40 (10), p.1511-1518

1997

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Pheochromocytoma in von Hippel-Lindau disease : Clinical presentation and mutation analysis in a large, multigenerational kindred

The journal of clinical endocrinology and metabolism, 1998, Vol.83 (1), p.117-120

1998

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Half-time of endogenous growth hormone (GH) disappearance in normal man after stimulation of GH secretion by GH-releasing hormone and suppression with somatostatin

The journal of clinical endocrinology and metabolism, 1989-03, Vol.68 (3), p.535-541

1989

Volltextzugriff (PDF)

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Treatment of Adrenocorticotropin-Dependent Cushing’s Syndrome: A Consensus Statement

Guidelines for Acromegaly Management: An Update

Diagnosis and Complications of Cushing’s Syndrome: A Consensus Statement

Consensus statement: medical management of acromegaly

Guidelines for Acromegaly Management

Surgical Management of GH-Secreting Pituitary Adenomas: An Outcome Study Using Modern Remission Criteria

Surgical management of GH-secreting pituitary adenomas: An outcome study using modern remission criteria

Growth Hormone Therapy in Adults and Children

Diagnosis and treatment of acromegaly complications

Radiosurgery for Cushing's disease after failed transsphenoidal surgery

The Pharmacokinetic and Pharmacodynamic Characteristics of a Long-Acting Growth Hormone (GH) Preparation (Nutropin Depot) in GH-Deficient Adults

Octreotide as primary therapy for acromegaly

Treatment of prolactin-secreting macroadenomas with the once-weekly dopamine agonist cabergoline

Enhanced basal and disorderly growth hormone secretion distinguish acromegalic from normal pulsatile growth hormone release

The antiviral compound enviroxime targets the 3A coding region of rhinovirus and poliovirus

Poliovirus 2C region functions during encapsidation of viral RNA

Radiosurgery for Pituitary Tumors and Craniopharyngiomas

Hypopituitarism

Temporal structure of in vivo growth hormone secretory events in humans

Cushing's disease resulting from pituitary corticotrophic microadenoma: Treatment results from transsphenoidal microsurgery and gamma knife radiosurgery

Sequence determinants of 3A-mediated resistance to enviroxime in rhinoviruses and enteroviruses

Evidence that enviroxime targets multiple components of the rhinovirus 14 replication complex

Synthesis, Antiviral Activity, and Biological Properties of Vinylacetylene Analogs of Enviroxime

Pheochromocytoma in von Hippel-Lindau disease : Clinical presentation and mutation analysis in a large, multigenerational kindred

Half-time of endogenous growth hormone (GH) disappearance in normal man after stimulation of GH secretion by GH-releasing hormone and suppression with somatostatin

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