LS Kirschner… - Nature genetics, 2000 - dir2.nichd.nih.gov 1Unit on Genetics & Endocrinology, Developmental Endocrinology Branch, National
Institute of Child Health and Human Development, 2Laboratory of Pathology,
National Cancer Institute, 3Cellular Biochemistry Section, Laboratory of ... Cited by 359 - Related articles - View as HTML - BL Direct - All 8 versions
- ►endojournals.org CA Stratakis, LS Kirschner, JA Carney - Journal of Clinical Endocrinology & Metabolism, 2001 - Endocrine Soc Carney complex is a multiple neoplasia syndrome featuring cardiac, endocrine,
cutaneous, and neural tumors, as well as a variety of pigmented lesions of the
skin and mucosae. Carney complex is inherited as an autosomal dominant ... Cited by 209 - Related articles - All 7 versions
- ►oxfordjournals.org LS Kirschner, F Sandrini, J Monbo, JP Lin, JA … - Human Molecular Genetics, 2000 - Oxford Univ Press Carney complex (CNC) is an autosomal dominant multiple neoplasia syndrome, which
has been linked to loci on 2p16 and 17q22–24. We recently reported that
PRKAR1A, which codes for the type 1A regulatory subunit of protein kinase A ... Cited by 174 - Related articles - BL Direct - All 8 versions
- ►endojournals.org A Lacroix, N N'Diaye, J Tremblay, P Hamet - Endocrine Reviews, 2001 - Endocrine Soc The mechanism by which cortisol is produced in adrenal Cushing's syndrome, when
ACTH is suppressed, was previously unknown and was referred to as being
"autonomous." More recently, several investigators have shown that some ... Cited by 173 - Related articles - BL Direct - All 4 versions
- ►angrylapdog.com CA Koch, K Pacak, GP Chrousos - Journal of Clinical Endocrinology & Metabolism, 2002 - jcem.endojournals.org.p.angrylapdog.com Modern imaging modalities lead to frequent detection of adrenal masses, most of
them incidental findings. Although the majority of adrenocortical and
adrenomedullary tumors are benign, there are no reliable clinical and ... Cited by 99 - Related articles - BL Direct - All 7 versions
- ►endojournals.org L Groussin, E Jullian, K Perlemoine, A Louvel … - Journal of Clinical Endocrinology & Metabolism, 2002 - Endocrine Soc Primary pigmented nodular adrenocortical disease (PPNAD) is a cause of
ACTH-independent Cushing's syndrome. This condition can be difficult to diagnose
because hypercortisolism may be periodic and adrenal imaging may not ... Cited by 79 - Related articles - BL Direct - All 4 versions
- ►aacrjournals.org J Bertherat, L Groussin, F Sandrini, L … - Cancer research, 2003 - AACR Germ-line protein kinase A (PKA) regulatory-subunit type-I (RI ;
PRKAR1A)-inactivating mutations and loss-of-heterozygosity (LOH) of its
17q22–24 locus have been found in Cushing syndrome (CS) caused by primary ... Cited by 78 - Related articles - BL Direct - All 4 versions
- ►nih.gov L Groussin, LS Kirschner, C Vincent-Dejean, K … - The American Journal of Human Genetics, 2002 - Elsevier We studied 11 new kindreds with primary pigmented nodular adrenocortical disease
(PPNAD) or Carney complex (CNC) and found that 82% of the kindreds had PRKAR1A
gene defects (including seven novel inactivating mutations), most of which ... Cited by 67 - Related articles - BL Direct - All 7 versions
- ►endojournals.org SD Pack, LS Kirschner, E Pak, Z Zhuang, JA … - Journal of Clinical Endocrinology & Metabolism, 2000 - Endocrine Soc Carney complex (CNC) is a familial multiple neoplasia and lentiginosis syndrome
with features overlapping those of McCune-Albright syndrome (MAS) and other
multiple endocrine neoplasia (MEN) syndromes, MEN type 1 (MEN 1), in ... Cited by 57 - Related articles - BL Direct - All 3 versions
I Bourdeau, SR Antonini, A Lacroix, LS … - Oncogene, 2004 - nature.com Corticotropin (ACTH)-independent macronodular adrenal hyperplasia (AIMAH) is a
heterogeneous condition in which cortisol secretion may be mediated by
gastrointestinal peptide (GIP), vasopressin, catecholamines and other ... Cited by 49 - Related articles - BL Direct - All 3 versions
