UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Chromosome 2 (2p16) abnormalities in Carney complex tumours

Journal of medical genetics, 2003-04, Vol.40 (4), p.268-277

2003

Volltextzugriff (PDF)

Genotypic heterogeneity and clinical phenotype in triple A syndrome: a review of the NIH experience 2000-2005

Clinical genetics, 2005-09, Vol.68 (3), p.215-221

2005

Volltextzugriff (PDF)

The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P450 aromatase gene transcription

The journal of clinical endocrinology and metabolism, 1998-04, Vol.83 (4), p.1348-1357

1998

Volltextzugriff (PDF)

Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes

Journal of endocrinological investigation, 2001-05, Vol.24 (5), p.370-383

STRATAKIS, C. A

2001

Volltextzugriff (PDF)

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2

The Journal of clinical investigation, 1996-02, Vol.97 (3), p.699-705

1996

Volltextzugriff (PDF)

Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex)

The journal of clinical endocrinology and metabolism, 1997-07, Vol.82 (7), p.2037-2043

1997

Volltextzugriff (PDF)

Segmental uniparental isodisomy (UPD) for 2p16 without clinical symptoms: implications for UPD and other genetic studies of chromosome 2

Journal of medical genetics, 2001-02, Vol.38 (2), p.106-109

2001

Volltextzugriff (PDF)

Male infertility as a component of Carney complex

Andrologia, 2007-10, Vol.39 (5), p.196-197

2007

Volltextzugriff (PDF)

Epithelioid blue nevus and psammomatous melanotic schwannoma: the unusual pigmented skin tumors of the Carney complex

Seminars in diagnostic pathology, 1998-08, Vol.15 (3), p.216-224

1998

Volltextzugriff (PDF)

Neurosurgical implications of Carney complex

Journal of neurosurgery, 2000-03, Vol.92 (3), p.413-418

2000

Volltextzugriff (PDF)

Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas (Carney complex)

The journal of clinical endocrinology and metabolism, 2000-10, Vol.85 (10), p.3860-3865

2000

Volltextzugriff (PDF)

Osteochondromyxoma of bone: a congenital tumor associated with lentigines and other unusual disorders

The American journal of surgical pathology, 2001-02, Vol.25 (2), p.164-176

2001

Volltextzugriff (PDF)

A syndrome of overgrowth and acromegaloidism with normal growth hormone secretion is associated with chromosome 11 pericentric inversion

Journal of medical genetics, 2001-05, Vol.38 (5), p.338-343

2001

Volltextzugriff (PDF)

Genetics of adrenocortical tumors : Carney complex

Annales d'endocrinologie, 2001-04, Vol.62 (2), p.180-184

STRATAKIS, C. A

2001

Volltextzugriff (PDF)

Synaptophysin immunoreactivity in primary pigmented nodular adrenocortical disease : Neuroendocrine properties of tumors associated with carney complex

The journal of clinical endocrinology and metabolism, 1999-03, Vol.84 (3), p.1122-1128

1999

Volltextzugriff (PDF)

Pigmented lesions of the conjunctiva in Carney’s complex

Journal of the American Academy of Dermatology, 2000-01, Vol.42 (1), p.145-145

2000

Volltextzugriff (PDF)

Carney Triad

Frontiers of hormone research, 2013, Vol.41, p.92-110

2013

Volltextzugriff (PDF)

Genetics of Peutz-Jeghers syndrome, Carney complex and other familial lentiginoses

Hormone research, 2000-01, Vol.54 (5-6), p.334-343

Stratakis, C A

2000

Volltextzugriff (PDF)

Ductal adenoma of the breast and the Carney complex

The American journal of surgical pathology, 1996-09, Vol.20 (9), p.1154

1996

Volltextzugriff (PDF)

Pituitary Adenoma in Carney Complex: An Immunohistochemical, Ultrastructural, and Immunoelectron Microscopic Study

Ultrastructural pathology, 2002-11, Vol.26 (6), p.345-353

2002

Volltextzugriff (PDF)

A mouse model for the carney complex tumor syndrome develops neoplasia in cyclic AMP-responsive tissues

Cancer research (Chicago, Ill.), 2005-06, Vol.65 (11), p.4506-4514

2005

Volltextzugriff (PDF)

Primary pigmented nodular adrenocortical disease: reevaluation of a patient with carney complex 27 years after unilateral adrenalectomy

The journal of clinical endocrinology and metabolism, 1997-04, Vol.82 (4), p.1274-1278

1997

Volltextzugriff (PDF)

Mutations of the Gene Encoding the Protein Kinase A Type I-α Regulatory Subunit (PRKAR1A) in Patients with the "Complex of Spotty Skin Pigmentation, Myxomas, Endocrine Overactivity, and Schwannomas" (Carney Complex)

Annals of the New York Academy of Sciences, 2002-06, Vol.968 (1), p.3-21

STRATAKIS, CONSTANTINE A.

2002

Volltextzugriff (PDF)

Carney Complex: Pathology and Molecular Genetics

Neuroendocrinology, 2006-01, Vol.83 (3-4), p.189-199

2006

Volltextzugriff (PDF)

Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gsα gene

Human genetics, 1996, Vol.98 (2), p.185-188

1996

Volltextzugriff (PDF)

1 – 25 von 44

Suche als RSS-Feed

Aktive Filter

ThemaSyndrome

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(39)
Mit Volltextzugriff
(34)

Publikationsform

Artikel
(43)
Buchkapitel
(1)

Sprache

Englisch
(44)

Erscheinungsjahr

n.n

Thema

Humans
(43)
Life Sciences & Biomedicine
(41)
Science & Technology
(41)
Male
(27)
Female
(26)
Biological And Medical Sciences
(17)
Endocrinology & Metabolism
(17)
Medical Sciences
(17)
Multiple Endocrine Neoplasia - Genetics
(14)
Adult
(13)
Carney Complex
(12)
Child
(12)
Genetics & Heredity
(12)
Middle Aged
(12)
Adolescent
(11)
Myxoma - Genetics
(11)
Myxoma - Pathology
(9)
Pigmentation Disorders - Genetics
(9)
Medical Genetics
(8)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Chromosome 2 (2p16) abnormalities in Carney complex tumours

Genotypic heterogeneity and clinical phenotype in triple A syndrome: a review of the NIH experience 2000-2005

The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P450 aromatase gene transcription

Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2

Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex)

Segmental uniparental isodisomy (UPD) for 2p16 without clinical symptoms: implications for UPD and other genetic studies of chromosome 2

Male infertility as a component of Carney complex

Epithelioid blue nevus and psammomatous melanotic schwannoma: the unusual pigmented skin tumors of the Carney complex

Neurosurgical implications of Carney complex

Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas (Carney complex)

Osteochondromyxoma of bone: a congenital tumor associated with lentigines and other unusual disorders

A syndrome of overgrowth and acromegaloidism with normal growth hormone secretion is associated with chromosome 11 pericentric inversion

Genetics of adrenocortical tumors : Carney complex

Synaptophysin immunoreactivity in primary pigmented nodular adrenocortical disease : Neuroendocrine properties of tumors associated with carney complex

Pigmented lesions of the conjunctiva in Carney’s complex

Carney Triad

Genetics of Peutz-Jeghers syndrome, Carney complex and other familial lentiginoses

Ductal adenoma of the breast and the Carney complex

Pituitary Adenoma in Carney Complex: An Immunohistochemical, Ultrastructural, and Immunoelectron Microscopic Study

A mouse model for the carney complex tumor syndrome develops neoplasia in cyclic AMP-responsive tissues

Primary pigmented nodular adrenocortical disease: reevaluation of a patient with carney complex 27 years after unilateral adrenalectomy

Mutations of the Gene Encoding the Protein Kinase A Type I-α Regulatory Subunit (PRKAR1A) in Patients with the "Complex of Spotty Skin Pigmentation, Myxomas, Endocrine Overactivity, and Schwannomas" (Carney Complex)

Carney Complex: Pathology and Molecular Genetics

Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gsα gene

Aktive Filter

Suchergebnisse filtern