S-LAM in a man: The first case report [1]

American Journal of Respiratory and Critical Care Medicine

Volumn 177, Issue 3, 2008, Pages 356-

  Sandrini, Alessandra ^a   Krishnan, Anu ^a   Yates, Deborah H ^a  

^a UNIVERSITY OF NEW SOUTH WALES   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL FEATURE; GENE MUTATION; HEALTH SURVEY; HUMAN; LETTER; LYMPHANGIOLEIOMYOMATOSIS; PRIORITY JOURNAL; QUESTIONNAIRE; TUBEROUS SCLEROSIS;

EID: 38849124096     PISSN: 1073449X     EISSN: 15354970     Source Type: Journal    
DOI: 10.1164/ajrccm.177.3.356     Document Type: Letter

References (3)

1. Schiavina M, Di Scioscio V, Contini P, Cavazza A, Fabiani A, Barberis M, Bini A, Altimari A, Cooke RMT, Grigioni WF, et al. Pulmonary lymphangioleiomyomatosis in a karyotypically normal man without tuberous sclerosis complex. Am J Respir Crit Care Med 2007;176:96-98.
2. McCormack FX, Moss J. S-LAM in a man? Am J Respir Crit Care Med 2007;176:3-4.
3. Dabora SL, Jozwiak S, Franz DN, Roberts PS, Nieto A, Chung J, Choy YS, Reeve MP, Thiele E, Egelhoff JC, et al. Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organs. Am J Hum Genet 2001;68:64-80.