Newman JH - Search Results

1

Mutation in the gene for bone morphogenetic protein receptor II as a cause of primary pulmonary hypertension in a large kindred.

Newman JH, Wheeler L, Lane KB, Loyd E, Gaddipati R, Phillips JA 3rd, Loyd JE. Newman JH, et al. N Engl J Med. 2001 Aug 2;345(5):319-24. doi: 10.1056/NEJM200108023450502. N Engl J Med. 2001. PMID: 11484688 Free article.

2

Pulmonary veno-occlusive disease caused by an inherited mutation in bone morphogenetic protein receptor II.

Runo JR, Vnencak-Jones CL, Prince M, Loyd JE, Wheeler L, Robbins IM, Lane KB, Newman JH, Johnson J, Nichols WC, Phillips JA 3rd. Runo JR, et al. Among authors: newman jh. Am J Respir Crit Care Med. 2003 Mar 15;167(6):889-94. doi: 10.1164/rccm.200208-861OC. Epub 2002 Nov 21. Am J Respir Crit Care Med. 2003. PMID: 12446270

3

Genetic basis of pulmonary arterial hypertension: current understanding and future directions.

Newman JH, Trembath RC, Morse JA, Grunig E, Loyd JE, Adnot S, Coccolo F, Ventura C, Phillips JA 3rd, Knowles JA, Janssen B, Eickelberg O, Eddahibi S, Herve P, Nichols WC, Elliott G. Newman JH, et al. J Am Coll Cardiol. 2004 Jun 16;43(12 Suppl S):33S-39S. doi: 10.1016/j.jacc.2004.02.028. J Am Coll Cardiol. 2004. PMID: 15194176 Free article. Review.

4

Serotonin transporter polymorphisms in familial and idiopathic pulmonary arterial hypertension.

Willers ED, Newman JH, Loyd JE, Robbins IM, Wheeler LA, Prince MA, Stanton KC, Cogan JA, Runo JR, Byrne D, Humbert M, Simonneau G, Sztrymf B, Morse JA, Knowles JA, Roberts KE, McElroy JJ, Barst RJ, Phillips JA 3rd. Willers ED, et al. Among authors: newman jh. Am J Respir Crit Care Med. 2006 Apr 1;173(7):798-802. doi: 10.1164/rccm.200509-1361OC. Epub 2005 Dec 9. Am J Respir Crit Care Med. 2006. PMID: 16339917 Free PMC article.

5

Narrative review: the enigma of pulmonary arterial hypertension: new insights from genetic studies.

Newman JH, Phillips JA 3rd, Loyd JE. Newman JH, et al. Ann Intern Med. 2008 Feb 19;148(4):278-83. doi: 10.7326/0003-4819-148-4-200802190-00006. Ann Intern Med. 2008. PMID: 18283205 Review.

6

Truncating and missense BMPR2 mutations differentially affect the severity of heritable pulmonary arterial hypertension.

Austin ED, Phillips JA, Cogan JD, Hamid R, Yu C, Stanton KC, Phillips CA, Wheeler LA, Robbins IM, Newman JH, Loyd JE. Austin ED, et al. Among authors: newman jh. Respir Res. 2009 Sep 28;10(1):87. doi: 10.1186/1465-9921-10-87. Respir Res. 2009. PMID: 19785764 Free PMC article.

7

Longitudinal analysis casts doubt on the presence of genetic anticipation in heritable pulmonary arterial hypertension.

Larkin EK, Newman JH, Austin ED, Hemnes AR, Wheeler L, Robbins IM, West JD, Phillips JA 3rd, Hamid R, Loyd JE. Larkin EK, et al. Among authors: newman jh. Am J Respir Crit Care Med. 2012 Nov 1;186(9):892-6. doi: 10.1164/rccm.201205-0886OC. Epub 2012 Aug 23. Am J Respir Crit Care Med. 2012. PMID: 22923661 Free PMC article.

8

Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension.

Loyd JE, Butler MG, Foroud TM, Conneally PM, Phillips JA 3rd, Newman JH. Loyd JE, et al. Among authors: newman jh. Am J Respir Crit Care Med. 1995 Jul;152(1):93-7. doi: 10.1164/ajrccm.152.1.7599869. Am J Respir Crit Care Med. 1995. PMID: 7599869 Free PMC article.

9

Genetics of primary pulmonary hypertension.

Thomas AQ, Gaddipati R, Newman JH, Loyd JE. Thomas AQ, et al. Among authors: newman jh. Clin Chest Med. 2001 Sep;22(3):477-91, ix. doi: 10.1016/s0272-5231(05)70285-9. Clin Chest Med. 2001. PMID: 11590842 Review.

10

An imbalance between the excretion of thromboxane and prostacyclin metabolites in pulmonary hypertension.

Christman BW, McPherson CD, Newman JH, King GA, Bernard GR, Groves BM, Loyd JE. Christman BW, et al. Among authors: newman jh. N Engl J Med. 1992 Jul 9;327(2):70-5. doi: 10.1056/NEJM199207093270202. N Engl J Med. 1992. PMID: 1603138 Free article.

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