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Items: 1 to 50 of 124

1.

Levetiracetam monotherapy in juvenile myoclonic epilepsy.

Sharpe DV, Patel AD, Abou-Khalil B, Fenichel GM.

Seizure. 2008 Jan;17(1):64-8. Epub 2007 Aug 9.

2.

Limb-girdle muscular dystrophy in the United States.

Moore SA, Shilling CJ, Westra S, Wall C, Wicklund MP, Stolle C, Brown CA, Michele DE, Piccolo F, Winder TL, Stence A, Barresi R, King N, King W, Florence J, Campbell KP, Fenichel GM, Stedman HH, Kissel JT, Griggs RC, Pandya S, Mathews KD, Pestronk A, Serrano C, Darvish D, Mendell JR.

J Neuropathol Exp Neurol. 2006 Oct;65(10):995-1003.

PMID:
17021404
3.

Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia.

Hedera P, Fenichel GM, Blair M, Haines JL.

Arch Neurol. 2004 Oct;61(10):1600-3.

PMID:
15477516
4.

Neurocutaneous syndromes.

Dahan D, Fenichel GM, El-Said R.

Adolesc Med. 2002 Oct;13(3):495-509. Review.

PMID:
12270797
5.

A randomized efficacy and safety trial of oxandrolone in the treatment of Duchenne dystrophy.

Fenichel GM, Griggs RC, Kissel J, Kramer TI, Mendell JR, Moxley RT, Pestronk A, Sheng K, Florence J, King WM, Pandya S, Robison VD, Wang H.

Neurology. 2001 Apr 24;56(8):1075-9.

PMID:
11320181
6.

Pediatric manifestations of Hashimoto's encephalopathy.

Vasconcellos E, PiƱa-Garza JE, Fakhoury T, Fenichel GM.

Pediatr Neurol. 1999 May;20(5):394-8. Review.

PMID:
10371389
7.
8.
9.

Chronic post-traumatic headache often a myth?

Warner JS, Fenichel GM.

Neurology. 1996 Apr;46(4):915-6. No abstract available.

PMID:
8780063
10.

Dystonia and unique muscle features. A 23-year follow-up and correction of diagnosis in two brothers.

Charles PD, Davis TL, Robertson D, Fenichel GM.

Arch Neurol. 1995 Aug;52(8):825-6.

PMID:
7639635
11.

Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita.

George AL Jr, Sloan-Brown K, Fenichel GM, Mitchell GA, Spiegel R, Pascuzzi RM.

Hum Mol Genet. 1994 Nov;3(11):2071-2. No abstract available.

PMID:
7874130
12.

Sneddon and antiphospholipid antibody syndromes causing bilateral thalamic infarction.

Charles PD, Fenichel GM.

Pediatr Neurol. 1994 May;10(3):262-3.

PMID:
8060434
13.

Thymectomy for the myasthenia gravis patient: factors influencing outcome.

Frist WH, Thirumalai S, Doehring CB, Merrill WH, Stewart JR, Fenichel GM, Bender HW Jr.

Ann Thorac Surg. 1994 Feb;57(2):334-8.

PMID:
8311593
14.

Three new mutations in patients with myophosphorylase deficiency (McArdle disease).

Tsujino S, Shanske S, Nonaka I, Eto Y, Mendell JR, Fenichel GM, DiMauro S.

Am J Hum Genet. 1994 Jan;54(1):44-52.

15.

Neurological examination of the newborn.

Fenichel GM.

Brain Dev. 1993 Nov-Dec;15(6):403-10. Review.

PMID:
8147498
16.

Prolongation of ambulation in children with Duchenne muscular dystrophy by subcutaneous lower limb tenotomy.

Smith SE, Green NE, Cole RJ, Robison JD, Fenichel GM.

J Pediatr Orthop. 1993 May-Jun;13(3):336-40.

PMID:
8496368
17.

Postvaccinal parkinsonism.

Fenichel GM.

Mov Disord. 1993 Apr;8(2):253. No abstract available.

PMID:
8097281
18.

Duchenne dystrophy: randomized, controlled trial of prednisone (18 months) and azathioprine (12 months)

Griggs RC, Moxley RT 3rd, Mendell JR, Fenichel GM, Brooke MH, Pestronk A, Miller JP, Cwik VA, Pandya S, Robison J, et al.

Neurology. 1993 Mar;43(3 Pt 1):520-7.

PMID:
8450994
19.

Long-term benefit from prednisone therapy in Duchenne muscular dystrophy.

Fenichel GM, Florence JM, Pestronk A, Mendell JR, Moxley RT 3rd, Griggs RC, Brooke MH, Miller JP, Robison J, King W, et al.

Neurology. 1991 Dec;41(12):1874-7.

PMID:
1745340
20.

Risk of seizures after measles-mumps-rubella immunization.

Griffin MR, Ray WA, Mortimer EA, Fenichel GM, Schaffner W.

Pediatrics. 1991 Nov;88(5):881-5.

PMID:
1945626
21.

A comparison of daily and alternate-day prednisone therapy in the treatment of Duchenne muscular dystrophy.

Fenichel GM, Mendell JR, Moxley RT 3rd, Griggs RC, Brooke MH, Miller JP, Pestronk A, Robison J, King W, Signore L, et al.

Arch Neurol. 1991 Jun;48(6):575-9.

PMID:
2039377
22.

Prednisone in Duchenne dystrophy. A randomized, controlled trial defining the time course and dose response. Clinical Investigation of Duchenne Dystrophy Group.

Griggs RC, Moxley RT 3rd, Mendell JR, Fenichel GM, Brooke MH, Pestronk A, Miller JP.

Arch Neurol. 1991 Apr;48(4):383-8.

PMID:
2012511
23.

Randomized, double-blind trial of mazindol in Duchenne dystrophy.

Griggs RC, Moxley RT 3rd, Mendell JR, Fenichel GM, Brooke MH, Miller PJ, Mandel S, Florence J, Schierbecker J, Kaiser KK, et al.

Muscle Nerve. 1990 Dec;13(12):1169-73.

PMID:
2266990
24.

Risk of seizures and encephalopathy after immunization with the diphtheria-tetanus-pertussis vaccine.

Griffin MR, Ray WA, Mortimer EA, Fenichel GM, Schaffner W.

JAMA. 1990 Mar 23-30;263(12):1641-5.

PMID:
2308203
25.

Pimozide treatment of Sydenham's chorea.

Shannon KM, Fenichel GM.

Neurology. 1990 Jan;40(1):186. No abstract available.

PMID:
2296371
26.

Testing of therapeutic interventions in humans.

Fenichel GM, Cooper DO, Brooke MH.

Muscle Nerve. 1990;13 Suppl:S1. No abstract available.

PMID:
2233873
27.

Adverse events following immunization: assessing probability of causation.

Fenichel GM, Lane DA, Livengood JR, Horwitz SJ, Menkes JH, Schwartz JF.

Pediatr Neurol. 1989 Sep-Oct;5(5):287-90.

PMID:
2803385
28.

Genetic forms of myasthenia gravis.

Misulis KE, Fenichel GM.

Pediatr Neurol. 1989 Jul-Aug;5(4):205-10. Review.

PMID:
2679583
29.

Myasthenia gravis.

Fenichel GM.

Pediatr Ann. 1989 Jul;18(7):432-8. Review. No abstract available.

PMID:
2666925
30.

Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy.

Mendell JR, Moxley RT, Griggs RC, Brooke MH, Fenichel GM, Miller JP, King W, Signore L, Pandya S, Florence J, et al.

N Engl J Med. 1989 Jun 15;320(24):1592-7.

PMID:
2657428
31.

Familial aplasia of the cerebellar vermis. Possible X-linked dominant inheritance.

Fenichel GM, Phillips JA.

Arch Neurol. 1989 May;46(5):582-3.

PMID:
2469415
32.

Duchenne muscular dystrophy: patterns of clinical progression and effects of supportive therapy.

Brooke MH, Fenichel GM, Griggs RC, Mendell JR, Moxley R, Florence J, King WM, Pandya S, Robison J, Schierbecker J, et al.

Neurology. 1989 Apr;39(4):475-81.

PMID:
2927672
33.

Clinical investigation in Duchenne muscular dystrophy: penicillamine and vitamin E.

Fenichel GM, Brooke MH, Griggs RC, Mendell JR, Miller JP, Moxley RT 3rd, Park JH, Provine MA, Florence J, Kaiser KK, et al.

Muscle Nerve. 1988 Nov;11(11):1164-8.

PMID:
3067086
34.

Congenital muscular dystrophies.

Fenichel GM.

Neurol Clin. 1988 Aug;6(3):519-28. Review.

PMID:
3065598
35.

Pertussis: the disease and the vaccine.

Fenichel GM.

Pediatr Neurol. 1988 Jul-Aug;4(4):201-6. Review.

PMID:
3072005
36.

Update: Duchenne muscular dystrophy.

Fenichel GM, Robison JD.

Compr Ther. 1988 Jul;14(7):29-32. Review. No abstract available.

PMID:
3060302
37.

Genetic heterogeneity in Duchenne dystrophy.

Hyser CL, Province M, Griggs RC, Mendell JR, Fenichel GM, Brooke MH, Miller JP, Polakowska R, Doherty RA, Quirk S, et al.

Ann Neurol. 1987 Oct;22(4):553-5.

PMID:
3435074
38.

Carrier assessment for mothers and sisters of isolated Duchenne dystrophy cases: the importance of serum enzyme determinations.

Hyser CL, Doherty RA, Griggs RC, Mendell JR, Polakowska R, Quirk S, Brooke MH, Fenichel GM.

Neurology. 1987 Sep;37(9):1476-80.

PMID:
2888052
39.

Clinical investigation of Duchenne muscular dystrophy. Interesting results in a trial of prednisone.

Brooke MH, Fenichel GM, Griggs RC, Mendell JR, Moxley RT 3rd, Miller JP, Kaiser KK, Florence JM, Pandya S, Signore L, et al.

Arch Neurol. 1987 Aug;44(8):812-7.

PMID:
3632393
40.

Clinical investigation of Duchenne muscular dystrophy. A methodology for therapeutic trials based on natural history controls.

Mendell JR, Province MA, Moxley RT 3rd, Griggs RC, Brooke MH, Fenichel GM, Miller JP, Kaiser KK, King W, Robison J, et al.

Arch Neurol. 1987 Aug;44(8):808-11.

PMID:
3115236
41.
42.

Superoxide dismutases, glutathione peroxidase, and catalase in neuromuscular disease.

Burr IM, Asayama K, Fenichel GM.

Muscle Nerve. 1987 Feb;10(2):150-4.

PMID:
3821787
43.

Clinical investigation in Duchenne dystrophy. VI. Double-blind controlled trial of nifedipine.

Moxley RT 3rd, Brooke MH, Fenichel GM, Mendell JR, Griggs RC, Miller JP, Province MA, Patterson V.

Muscle Nerve. 1987 Jan;10(1):22-33.

PMID:
3550455
44.

Use of serum creatine kinase, pyruvate kinase, and genetic linkage for carrier detection in Duchenne and Becker dystrophy.

Hyser CL, Griggs RC, Mendell JR, Polakowska R, Quirk S, Brooke MH, Fenichel GM, Doherty RA.

Neurology. 1987 Jan;37(1):4-10.

PMID:
2879259
45.

Diffuse retinopathy following measles, mumps, and rubella vaccination.

Marshall GS, Wright PF, Fenichel GM, Karzon DT.

Pediatrics. 1985 Dec;76(6):989-91. No abstract available.

PMID:
4069871
46.

Valproate hepatotoxicity: two new cases, a summary of others, and recommendations.

Fenichel GM, Greene HL.

Pediatr Neurol. 1985 Mar-Apr;1(2):109-13. Review.

PMID:
3939742
47.

Migraine in children.

Fenichel GM.

Neurol Clin. 1985 Feb;3(1):77-94. Review.

PMID:
3887129
48.

Clinical investigation in Duchenne dystrophy: V. Use of creatine kinase and pyruvate kinase in carrier detection.

Griggs RC, Mendell JR, Brooke MH, Fenichel GM, Miller JP, Province M, Moxley RT 3rd, Huntzinger D, Vaughn A, Cohen M, et al.

Muscle Nerve. 1985 Jan;8(1):60-7.

PMID:
4058458
49.

Epidural hematoma of the newborn due to birth trauma.

Gama CH, Fenichel GM.

Pediatr Neurol. 1985 Jan-Feb;1(1):52-3.

PMID:
3880390
50.

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