- ►annals.org [PDF] CA Stratakis, N Sarlis, LS Kirschner, JA … - Annals of internal medicine, 1999 - Am Coll Physicians Constantine A. Stratakis, MD, DSc; Nicholas Sarlis, MD, PhD; Lawrence S.
Kirschner, MD, PhD; J. Aidan Carney, MD, PhD; John L. Doppman, MD; Lynnette K.
Nieman, MD; George P. Chrousos, MD; and Dimitris A. Papanicolaou, MD Cited by 85 - Related articles - BL Direct - All 4 versions
JA Carney, WF Young Jr - The Endocrinologist, 1992 - journals.lww.com Artide 0O21.972X/92/7OOl-OO95$2 00/0 The Endocrinologist Copyright .с 1992 by
Williams& Wilkins Primary Pigmented Nodular Adrenocortical Disease and Its
Associated Conditions J. Aidan Carney, MD, PhD., FRCPI,* & William F. ... Cited by 95 - Related articles
- ►endojournals.org NJ Sarlis, GP Chrousos, JL Doppman, JA … - Journal of Clinical Endocrinology & Metabolism, 1997 - Endocrine Soc This patient's early growth and development were normal. In 1958, at the age of
7 yr, he was referred for investigation of isosexual precocious puberty. No
specific cause was identified, although his bone age was advanced. The ... Cited by 54 - Related articles - BL Direct - All 3 versions
- ►endojournals.org I Bourdeau, A Lacroix, W Schurch, P Caron, T … - Journal of Clinical Endocrinology & Metabolism, 2003 - Endocrine Soc Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of
ACTH-independent adrenal Cushing's syndrome (CS), which is often associated with
Carney complex (CNC). We have recently described a paradoxical increase in ... Cited by 30 - Related articles - BL Direct - All 3 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
DF Gunther, I Bourdeau, L Matyakhina, D … - Journal of Clinical Endocrinology & Metabolism, 2004 - Endocrine Soc Cushing syndrome is uncommon in childhood and rare in infancy. We report the
case of a 3-yr-old child who presented with symptoms of Cushing syndrome
beginning shortly after birth. Her hypercortisolemia was cyclical, causing ... Cited by 37 - Related articles - All 5 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
- ►endojournals.org CA Stratakis, NA Courcoutsakis, A Abati, A … - Journal of Clinical Endocrinology & Metabolism, 1997 - Endocrine Soc Carney complex is a multiple neoplasia and lentiginosis syndrome that affects
endocrine glands, including the pituitary, adrenals, and testes; thyroid gland
involvement has not been unequivocally demonstrated. In the present study, ... Cited by 102 - Related articles - BL Direct - All 5 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
- ►ahajournals.org M Casey, C Mah, AD Merliss, LS Kirschner, SE … - Circulation, 1998 - Am Heart Assoc From the Cardiology Division, Department of Medicine and Department of Cell
Biology and Anatomy, Cornell University Medical College, The New York Hospital,
New York, NY (MC, CM, CTB); Pacing and Electrophysiology, MeritCare Heart ... Cited by 130 - Related articles - BL Direct - All 5 versions
