Gahl WA - Search Results

1

Aortic stenosis and vascular calcifications in alkaptonuria.

Hannoush H, Introne WJ, Chen MY, Lee SJ, O'Brien K, Suwannarat P, Kayser MA, Gahl WA, Sachdev V. Hannoush H, et al. Among authors: gahl wa. Mol Genet Metab. 2012 Feb;105(2):198-202. doi: 10.1016/j.ymgme.2011.10.017. Epub 2011 Oct 30. Mol Genet Metab. 2012. PMID: 22100375 Free PMC article.

2

Clinical, molecular, and cell biological aspects of Chediak-Higashi syndrome.

Introne W, Boissy RE, Gahl WA. Introne W, et al. Among authors: gahl wa. Mol Genet Metab. 1999 Oct;68(2):283-303. doi: 10.1006/mgme.1999.2927. Mol Genet Metab. 1999. PMID: 10527680 Review.

3

Exacerbation of the ochronosis of alkaptonuria due to renal insufficiency and improvement after renal transplantation.

Introne WJ, Phornphutkul C, Bernardini I, McLaughlin K, Fitzpatrick D, Gahl WA. Introne WJ, et al. Among authors: gahl wa. Mol Genet Metab. 2002 Sep-Oct;77(1-2):136-42. doi: 10.1016/s1096-7192(02)00121-x. Mol Genet Metab. 2002. PMID: 12359141

4

Natural history of alkaptonuria.

Phornphutkul C, Introne WJ, Perry MB, Bernardini I, Murphey MD, Fitzpatrick DL, Anderson PD, Huizing M, Anikster Y, Gerber LH, Gahl WA. Phornphutkul C, et al. Among authors: gahl wa. N Engl J Med. 2002 Dec 26;347(26):2111-21. doi: 10.1056/NEJMoa021736. N Engl J Med. 2002. PMID: 12501223 Free article.

5

Minocycline-induced hyperpigmentation masquerading as alkaptonuria in individuals with joint pain.

Suwannarat P, Phornphutkul C, Bernardini I, Turner M, Gahl WA. Suwannarat P, et al. Among authors: gahl wa. Arthritis Rheum. 2004 Nov;50(11):3698-701. doi: 10.1002/art.20606. Arthritis Rheum. 2004. PMID: 15529343 Free article.

6

Blue pigmentation and arthritis in an elderly man.

Spenny ML, Suwannarat P, Gahl WA, Cowen EW. Spenny ML, et al. Among authors: gahl wa. J Am Acad Dermatol. 2005 Jan;52(1):122-4. doi: 10.1016/j.jaad.2004.09.011. J Am Acad Dermatol. 2005. PMID: 15627089 No abstract available.

7

Two novel CHS1 (LYST) mutations: clinical correlations in an infant with Chediak-Higashi syndrome.

Zarzour W, Kleta R, Frangoul H, Suwannarat P, Jeong A, Kim SY, Wayne AS, Gunay-Aygun M, White J, Filipovich AH, Gahl WA. Zarzour W, et al. Among authors: gahl wa. Mol Genet Metab. 2005 Jun;85(2):125-32. doi: 10.1016/j.ymgme.2005.02.011. Epub 2005 Mar 25. Mol Genet Metab. 2005. PMID: 15896657

8

Use of nitisinone in patients with alkaptonuria.

Suwannarat P, O'Brien K, Perry MB, Sebring N, Bernardini I, Kaiser-Kupfer MI, Rubin BI, Tsilou E, Gerber LH, Gahl WA. Suwannarat P, et al. Among authors: gahl wa. Metabolism. 2005 Jun;54(6):719-28. doi: 10.1016/j.metabol.2004.12.017. Metabolism. 2005. PMID: 15931605

9

Single nucleotide polymorphisms in the dystroglycan gene do not correlate with disease severity in hereditary inclusion body myopathy.

Gottlieb E, Ciccone C, Darvish D, Naiem-Cohen S, Dalakas MC, Savelkoul PJ, Krasnewich DM, Gahl WA, Huizing M. Gottlieb E, et al. Among authors: gahl wa. Mol Genet Metab. 2005 Sep-Oct;86(1-2):244-9. doi: 10.1016/j.ymgme.2005.07.003. Mol Genet Metab. 2005. PMID: 16112887

10

Nodular regenerative hyperplasia and severe portal hypertension in cystinosis.

O'Brien K, Hussain N, Warady BA, Kleiner DE, Kleta R, Bernardini I, Heller T, Gahl WA. O'Brien K, et al. Among authors: gahl wa. Clin Gastroenterol Hepatol. 2006 Mar;4(3):387-94. doi: 10.1016/j.cgh.2005.12.013. Clin Gastroenterol Hepatol. 2006. PMID: 16527704

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