Brantly ML - Search Results

1

Association of IREB2 and CHRNA3 polymorphisms with airflow obstruction in severe alpha-1 antitrypsin deficiency.

Kim WJ, Wood AM, Barker AF, Brantly ML, Campbell EJ, Eden E, McElvaney G, Rennard SI, Sandhaus RA, Stocks JM, Stoller JK, Strange C, Turino G, Silverman EK, Stockley RA, Demeo DL. Kim WJ, et al. Among authors: brantly ml. Respir Res. 2012 Feb 22;13(1):16. doi: 10.1186/1465-9921-13-16. Respir Res. 2012. PMID: 22356581 Free PMC article.

2

Clinical features and history of the destructive lung disease associated with alpha-1-antitrypsin deficiency of adults with pulmonary symptoms.

Brantly ML, Paul LD, Miller BH, Falk RT, Wu M, Crystal RG. Brantly ML, et al. Am Rev Respir Dis. 1988 Aug;138(2):327-36. doi: 10.1164/ajrccm/138.2.327. Am Rev Respir Dis. 1988. PMID: 3264124

3

Clinical features of individuals with PI*SZ phenotype of alpha 1-antitrypsin deficiency. alpha 1-Antitrypsin Deficiency Registry Study Group.

Turino GM, Barker AF, Brantly ML, Cohen AB, Connelly RP, Crystal RG, Eden E, Schluchter MD, Stoller JK. Turino GM, et al. Among authors: brantly ml. Am J Respir Crit Care Med. 1996 Dec;154(6 Pt 1):1718-25. doi: 10.1164/ajrccm.154.6.8970361. Am J Respir Crit Care Med. 1996. PMID: 8970361

4

Baseline characteristics of enrollees in the National Heart, Lung and Blood Institute Registry of alpha 1-antitrypsin deficiency. Alpha 1-Antitrypsin Deficiency Registry Study Group.

McElvaney NG, Stoller JK, Buist AS, Prakash UB, Brantly ML, Schluchter MD, Crystal RD. McElvaney NG, et al. Among authors: brantly ml. Chest. 1997 Feb;111(2):394-403. doi: 10.1378/chest.111.2.394. Chest. 1997. PMID: 9041988

5

Endothelial nitric oxide synthase as a potential susceptibility gene in the pathogenesis of emphysema in alpha1-antitrypsin deficiency.

Novoradovsky A, Brantly ML, Waclawiw MA, Chaudhary PP, Ihara H, Qi L, Eissa NT, Barnes PM, Gabriele KM, Ehrmantraut ME, Rogliani P, Moss J. Novoradovsky A, et al. Among authors: brantly ml. Am J Respir Cell Mol Biol. 1999 Mar;20(3):441-7. doi: 10.1165/ajrcmb.20.3.3144. Am J Respir Cell Mol Biol. 1999. PMID: 10030842

6

Formation and current results of a patient-organized registry for alpha(1)-antitrypsin deficiency.

Stoller JK, Brantly M, Fleming LE, Bean JA, Walsh J. Stoller JK, et al. Chest. 2000 Sep;118(3):843-8. doi: 10.1378/chest.118.3.843. Chest. 2000. PMID: 10988213

7

Biochemical efficacy and safety of a new pooled human plasma alpha(1)-antitrypsin, Respitin.

Stoller JK, Rouhani F, Brantly M, Shahin S, Dweik RA, Stocks JM, Clausen J, Campbell E, Norton F. Stoller JK, et al. Chest. 2002 Jul;122(1):66-74. doi: 10.1378/chest.122.1.66. Chest. 2002. PMID: 12114340 Clinical Trial.

8

Asthma features in severe alpha1-antitrypsin deficiency: experience of the National Heart, Lung, and Blood Institute Registry.

Eden E, Hammel J, Rouhani FN, Brantly ML, Barker AF, Buist AS, Fallat RJ, Stoller JK, Crystal RG, Turino GM. Eden E, et al. Among authors: brantly ml. Chest. 2003 Mar;123(3):765-71. doi: 10.1378/chest.123.3.765. Chest. 2003. PMID: 12628876

9

Genetic testing for alpha1-antitrypsin deficiency.

Strange C, Dickson R, Carter C, Carpenter MJ, Holladay B, Lundquist R, Brantly ML. Strange C, et al. Among authors: brantly ml. Genet Med. 2004 Jul-Aug;6(4):204-10. doi: 10.1097/01.gim.0000132669.09819.79. Genet Med. 2004. PMID: 15266208 Free article.

10

[American Thoracic Society/European Respiratory Society Statement: Standards for the diagnosis and management of individuals with alpha-1 antitrypsin deficiency].

Stoller JK, Snider GL, Brantly ML, Fallat RJ, Stockley RA, Turino GM, Konietzko N, Dirksen A, Eden E, Fallat RJ, Luisetti M, Stolk J, Strange C; American Thoracic Society; European Respiratory Society. Stoller JK, et al. Among authors: brantly ml. Pneumologie. 2005 Jan;59(1):36-68. doi: 10.1055/s-2004-830176. Pneumologie. 2005. PMID: 15685488 German. No abstract available.

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