Chuck G - Search Results

1

Pulmonary cysts consistent with lymphangioleiomyomatosis are common in women with tuberous sclerosis: genetic and radiographic analysis.

McCormack F, Brody A, Meyer C, Leonard J, Chuck G, Dabora S, Sethuraman G, Colby TV, Kwiatkowski DJ, Franz DN. McCormack F, et al. Among authors: chuck g. Chest. 2002 Mar;121(3 Suppl):61S. Chest. 2002. PMID: 11893688 No abstract available.

2

Mutational and radiographic analysis of pulmonary disease consistent with lymphangioleiomyomatosis and micronodular pneumocyte hyperplasia in women with tuberous sclerosis.

Franz DN, Brody A, Meyer C, Leonard J, Chuck G, Dabora S, Sethuraman G, Colby TV, Kwiatkowski DJ, McCormack FX. Franz DN, et al. Among authors: chuck g. Am J Respir Crit Care Med. 2001 Aug 15;164(4):661-8. doi: 10.1164/ajrccm.164.4.2011025. Am J Respir Crit Care Med. 2001. PMID: 11520734

3

Rapamycin causes regression of astrocytomas in tuberous sclerosis complex.

Franz DN, Leonard J, Tudor C, Chuck G, Care M, Sethuraman G, Dinopoulos A, Thomas G, Crone KR. Franz DN, et al. Among authors: chuck g. Ann Neurol. 2006 Mar;59(3):490-8. doi: 10.1002/ana.20784. Ann Neurol. 2006. PMID: 16453317

4

Levetiracetam as adjunctive antiepileptic therapy for patients with tuberous sclerosis complex: a retrospective open-label trial.

Collins JJ, Tudor C, Leonard JM, Chuck G, Franz DN. Collins JJ, et al. Among authors: chuck g. J Child Neurol. 2006 Jan;21(1):53-7. doi: 10.1177/08830738060210011201. J Child Neurol. 2006. PMID: 16551454

5

Sirolimus for angiomyolipoma in tuberous sclerosis complex or lymphangioleiomyomatosis.

Bissler JJ, McCormack FX, Young LR, Elwing JM, Chuck G, Leonard JM, Schmithorst VJ, Laor T, Brody AS, Bean J, Salisbury S, Franz DN. Bissler JJ, et al. Among authors: chuck g. N Engl J Med. 2008 Jan 10;358(2):140-51. doi: 10.1056/NEJMoa063564. N Engl J Med. 2008. PMID: 18184959 Free PMC article. Clinical Trial.

6

Glycine decarboxylase mutations: a distinctive phenotype of nonketotic hyperglycinemia in adults.

Dinopoulos A, Kure S, Chuck G, Sato K, Gilbert DL, Matsubara Y, Degrauw T. Dinopoulos A, et al. Among authors: chuck g. Neurology. 2005 Apr 12;64(7):1255-7. doi: 10.1212/01.WNL.0000156800.23776.40. Neurology. 2005. PMID: 15824356

7

Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle.

Bissler JJ, Tsoras M, Göring HH, Hug P, Chuck G, Tombragel E, McGraw C, Schlotman J, Ralston MA, Hug G. Bissler JJ, et al. Among authors: chuck g. Lab Invest. 2002 Mar;82(3):335-44. doi: 10.1038/labinvest.3780427. Lab Invest. 2002. PMID: 11896212 Free article.

8

Irreversible brain creatine deficiency with elevated serum and urine creatine: a creatine transporter defect?

Cecil KM, Salomons GS, Ball WS Jr, Wong B, Chuck G, Verhoeven NM, Jakobs C, DeGrauw TJ. Cecil KM, et al. Among authors: chuck g. Ann Neurol. 2001 Mar;49(3):401-4. doi: 10.1002/ana.79. Ann Neurol. 2001. PMID: 11261517

9

Presence of normal creatine in the muscle of a patient with a mutation in the creatine transporter: a case study.

Pyne-Geithman GJ, deGrauw TJ, Cecil KM, Chuck G, Lyons MA, Ishida Y, Clark JF. Pyne-Geithman GJ, et al. Among authors: chuck g. Mol Cell Biochem. 2004 Jul;262(1-2):35-9. doi: 10.1023/b:mcbi.0000038213.15646.4a. Mol Cell Biochem. 2004. PMID: 15532707

10

Congenital creatine transporter deficiency.

deGrauw TJ, Salomons GS, Cecil KM, Chuck G, Newmeyer A, Schapiro MB, Jakobs C. deGrauw TJ, et al. Among authors: chuck g. Neuropediatrics. 2002 Oct;33(5):232-8. doi: 10.1055/s-2002-36743. Neuropediatrics. 2002. PMID: 12536364

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