De Girolami U - Search Results

1

Rutkove SB, De Girolami U, Preston DC, Freeman R, Nardin RA, Gouras GK, Johns DR, Raynor EM. Rutkove SB, et al. Among authors: de girolami u. Muscle Nerve. 1996 Jul;19(7):870-5. doi: 10.1002/(SICI)1097-4598(199607)19:7<870::AID-MUS9>3.0.CO;2-6. Muscle Nerve. 1996. PMID: 8965841

2

Lovastatin/gemfibrozil myopathy: a clinical, histochemical, and ultrastructural study.

Chucrallah A, De Girolami U, Freeman R, Federman M. Chucrallah A, et al. Among authors: de girolami u. Eur Neurol. 1992;32(5):293-6. doi: 10.1159/000116845. Eur Neurol. 1992. PMID: 1521554

3

Endothelial dysfunction and the expression of endothelial nitric oxide synthetase in diabetic neuropathy, vascular disease, and foot ulceration.

Veves A, Akbari CM, Primavera J, Donaghue VM, Zacharoulis D, Chrzan JS, DeGirolami U, LoGerfo FW, Freeman R. Veves A, et al. Diabetes. 1998 Mar;47(3):457-63. doi: 10.2337/diabetes.47.3.457. Diabetes. 1998. PMID: 9519754

4

Pseudallescheria boydii infection of the central nervous system.

Kershaw P, Freeman R, Templeton D, DeGirolami PC, DeGirolami U, Tarsy D, Hoffmann S, Eliopoulos G, Karchmer AW. Kershaw P, et al. Arch Neurol. 1990 Apr;47(4):468-72. doi: 10.1001/archneur.1990.00530040126029. Arch Neurol. 1990. PMID: 2181980 Review.

5

Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy.

Mehta P, Küspert M, Bale T, Brownstein CA, Towne MC, De Girolami U, Shi J, Beggs AH, Darras BT, Wegner M, Piao X, Agrawal PB. Mehta P, et al. Among authors: de girolami u. Muscle Nerve. 2017 May;55(5):761-765. doi: 10.1002/mus.25416. Epub 2017 Feb 3. Muscle Nerve. 2017. PMID: 27668699 Free PMC article.

6

Inflammatory myopathy causing pharyngeal dysphagia: a new entity.

Shapiro J, Martin S, DeGirolami U, Goyal R. Shapiro J, et al. Ann Otol Rhinol Laryngol. 1996 May;105(5):331-5. doi: 10.1177/000348949610500501. Ann Otol Rhinol Laryngol. 1996. PMID: 8651624

7

Hereditary ataxia with sensory neuronopathy: Biemond's ataxia.

Nachmanoff DB, Segal RA, Dawson DM, Brown RB, De Girolami U. Nachmanoff DB, et al. Among authors: de girolami u. Neurology. 1997 Jan;48(1):273-5. doi: 10.1212/wnl.48.1.273. Neurology. 1997. PMID: 9008534

8

Expanding the phenotype associated with the NEFL mutation: neuromuscular disease in a family with overlapping myopathic and neurogenic findings.

Agrawal PB, Joshi M, Marinakis NS, Schmitz-Abe K, Ciarlini PD, Sargent JC, Markianos K, De Girolami U, Chad DA, Beggs AH. Agrawal PB, et al. Among authors: de girolami u. JAMA Neurol. 2014 Nov;71(11):1413-20. doi: 10.1001/jamaneurol.2014.1432. JAMA Neurol. 2014. PMID: 25264603 Free PMC article.

9

Transcriptional therapy with the histone deacetylase inhibitor trichostatin A ameliorates experimental autoimmune encephalomyelitis.

Camelo S, Iglesias AH, Hwang D, Due B, Ryu H, Smith K, Gray SG, Imitola J, Duran G, Assaf B, Langley B, Khoury SJ, Stephanopoulos G, De Girolami U, Ratan RR, Ferrante RJ, Dangond F. Camelo S, et al. Among authors: de girolami u. J Neuroimmunol. 2005 Jul;164(1-2):10-21. doi: 10.1016/j.jneuroim.2005.02.022. J Neuroimmunol. 2005. PMID: 15885809

10

BK-related polyomavirus vasculopathy in a renal-transplant recipient.

Petrogiannis-Haliotis T, Sakoulas G, Kirby J, Koralnik IJ, Dvorak AM, Monahan-Earley R, DE Girolami PC, DE Girolami U, Upton M, Major EO, Pfister LA, Joseph JT. Petrogiannis-Haliotis T, et al. Among authors: de girolami pc, de girolami u. N Engl J Med. 2001 Oct 25;345(17):1250-5. doi: 10.1056/NEJMoa010319. N Engl J Med. 2001. PMID: 11680445 Free article. No abstract available.

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