An X-traordinary stroke

The Lancet

Volumn 377, Issue 9773, 2011, Pages 1288-

  Verma, Shilpa ^a   Lewis, Diana ^a   Warne, Garry ^b   Grossmann, Mathis ^a,b,c  

^a EASTERN HEALTH   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c AUSTIN HEALTH   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROSTENEDIONE; CORTICOTROPIN; GLUCOCORTICOID; HYDROCORTISONE; HYDROXYPROGESTERONE; STEROID 21 MONOOXYGENASE;

ADULT; ARTICLE; ATAXIA; CASE REPORT; CEREBELLUM INFARCTION; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL ADRENAL HYPERPLASIA; DIPLOPIA; HUMAN; HUMAN TISSUE; MALE; POLYCYTHEMIA; PRIORITY JOURNAL; STEROID 21 MONOOXYGENASE DEFICIENCY; STROKE;

EID: 79953756083     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(10)62266-0     Document Type: Article

References (4)

1. PW Speiser, R Azziz, LS Baskin Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline J Clin Endocrinol Metab 95 2010 4133 4160
2. AT Nguyen, JJ Brown, GL Warne Growth in congenital adrenal hyperplasia Indian J Pediatr 73 2006 89 93 (Pubitemid 44323883)
3. MM Albareda, J Rodriguez-Espinosa, A Remacha, N Prat, SM Webb Polycythemia in a patient with 21-hydroxylase deficiency Haematologica 85 2000 e08
4. AP Gold, AF Michael Jr. Congenital adrenal hyperplasia associated with polycythemia Pediatrics 23 1959 727 730