A. Weber

发表

Are activating mutations of the adrenocorticotropin receptor involved in adrenal cortical neoplasia?

S. Asa, R. Clayton, A. Clark, 1995, Life sciences.

Adrenocorticotropin insensitivity syndromes.

A. Clark, A. Weber, A. Clark, 1998, Endocrine reviews.

The molecular pathology of pituitary hormone deficiency and resistance.

A. Clark, A. Weber, K. Woods, 1995, Bailliere's clinical endocrinology and metabolism.

Absence of mutations in the MEN2A region of the ret proto‐oncogene in non‐MEN 2A phaeochromocytomas

S. Chew, R. Ross, A. Clark, 1995, Clinical endocrinology.

Mutations of the ACTH receptor gene are only one cause of familial glucocorticoid deficiency.

A. Clark, A. Weber, Adrian J.L.Clark, 1994, Human molecular genetics.

Diminished adrenal androgen secretion in familial glucocorticoid deficiency implicates a significant role for ACTH in the induction of adrenarche

M. Savage, J. Honour, M. Savage, 1997, Clinical endocrinology.

Adrenocorticotropin receptor gene mutations in familial glucocorticoid deficiency: relationships with clinical features in four families.

J. Toppari, K. Näntö-Salonen, A. Clark, 1995, The Journal of clinical endocrinology and metabolism.

Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster.

H J Dean, T. Wienker, D. Easton, 1996, Human molecular genetics.

Molecular insights into inherited ACTH resistance syndromes

A. Clark, A. Weber, 1994, Trends in Endocrinology & Metabolism.

Familial glucocorticoid deficiency: one syndrome, but more than one gene

A. Clark, F. Cammas, S. Kapas, 1997, Journal of Molecular Medicine.

Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuria

J. Hennermann, A. Weber, E. Mönch, 2004, Journal of perinatal medicine.

Functional characterization of the cloned human ACTH receptor: impaired responsiveness of a mutant receptor in familial glucocorticoid deficiency.

A. Clark, D. Grant, S. Kapas, 1993, Biochemical and biophysical research communications.

Exclusion of the adrenocorticotropin (ACTH) receptor (MC2R) locus in some families with ACTH resistance but no mutations of the MC2R coding sequence (familial glucocorticoid deficiency type 2).

E. Génin, A. Clark, D. Naville, 1998, The Journal of clinical endocrinology and metabolism.

Adrenocorticotropin insensitivity syndromes.

A Weber, A J Clark, A. Weber, 1998, Endocrine reviews.

Magnetic resonance imaging of adrenocortical adenomas in childhood: Correlation with computed tomography and ultrasound

R. Reznek, P. Armstrong, M. Savage, 1996, Pediatric Radiology.