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378


Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations

Clark, Lorraine N; Afridi, Shehla; Mejia-Santana, Helen; Harris, Juliette; Louis, Elan D; Cote, Lucien J; Andrews, Howard; Singleton, Andrew; Wavrant De-Vrieze, Fabienne; Hardy, John; Mayeux, Richard; Fahn, Stanley; Waters, Cheryl; Ford, Blair; Frucht, Steven; Ottman, Ruth; Marder, Karen
The frequency and relative contribution of DJ-1 mutations in early-onset Parkinson's disease (EOPD) is currently unknown. We analyzed a cohort of 89 EOPD patients (mean age at onset of PD +/- SD, 41.5 +/- 7.2 years), ascertained independent of family history, who participated in a study of the genetic epidemiology of PD. This study includes sequence analysis of the DJ-1 gene in addition to assaying the 14,082-bp deletion spanning exons 1 to 5, previously identified in a Dutch kindred, in 89 EOPD cases. A heterozygous missense mutation in exon 5 (A104T) was identified in an EOPD case of Asian ethnicity; this sequence variant was absent in 308 control chromosomes. We identified additional sequence variation in the DJ-1 gene, including a polymorphism in the coding region in exon 5 (R98Q), three polymorphisms in the 5' untranslated region (exon 1A/1B), and two polymorphisms in intronic regions (IVS1 and IVS5). Mutations in the DJ-1 gene are rare in EOPD in both sporadic and familial cases.
PMID: 15254937
ISSN: 0885-3185
CID: 2761912

Levetiracetam as an anti-myoclonic agent [Meeting Abstract]

Wu, S; Frucht, S
ISI:000222500400495
ISSN: 0340-5354
CID: 2763532

Diagnosis and management of pergolide-induced fibrosis [Case Report]

Agarwal, Pinky; Fahn, Stanley; Frucht, Steven J
We report on 2 patients treated with pergolide, 1 of whom developed pleural fibrosis and the other retroperitoneal fibrosis. In both cases, an extensive diagnostic evaluation and surgical intervention were required to reach a diagnosis. Based on our experience with these patients and a review of cases of pergolide-induced fibrosis in the English-language literature, we propose guidelines for the diagnosis and management of this rare complication.
PMID: 15197712
ISSN: 0885-3185
CID: 2760992

The metabolic topography of posthypoxic myoclonus

Frucht, Steven J; Trost, Maja; Ma, Yilong; Eidelberg, David
Posthypoxic myoclonus (PHM) is a syndrome of action and intention myoclonus that occurs in some patients who survive a cardiac arrest. Using PET and statistical parametric mapping, the authors observed a significant bilateral increase in glucose metabolism in the ventrolateral thalamus and pontine tegmentum in patients relative to controls. Interventions such as deep brain stimulation that interrupt networks that involve these structures may be useful in patients with severe PHM
PMID: 15159501
ISSN: 1526-632X
CID: 93254

Movement disorder emergencies in the perioperative period

Frucht, Steven J
Movement disorder emergencies are uncommon in the perioperative period; however, when they occur, then carry significant morbidity. By paying attention to the phenomenology of the movement disorder, the effects of medications administered in the operating room, and unusual sequelae of surgery, neurologists can have a positive impact on the outcome of these patients.
PMID: 15062518
ISSN: 0733-8619
CID: 2761002

Designing the ideal movement disorders fellowship training program: The Columbia University experience 2001-2002 [Meeting Abstract]

Portera-Cailliau, C; Victor, D; Frucht, SJ; Fahn, S
ISI:000220761900203
ISSN: 0028-3878
CID: 2763452

The usefulness of FDG-PET in the differential diagnosis of parkinsonian disorders - An evidence based medicine like approach [Meeting Abstract]

Eckert, T; Barnes, A; Frucht, S; Dhawan, V; Gordon, MF; Eidelberg, D
ISI:000220761901278
ISSN: 0028-3878
CID: 2763462

Cerebrotendinous xanthomatosis masquerading as Friedreich's ataxia [Meeting Abstract]

Wu, SS; Heier, L; Frucht, SJ
ISI:000221639600073
ISSN: 0885-3185
CID: 2763472

Paroxysmal ballism in dizygotic twins: An unusual form of PNKD [Meeting Abstract]

Bordelon, YM; Leary, L; Frucht, S
ISI:000221639600159
ISSN: 0885-3185
CID: 2763482

Classification conundrums in paroxysmal dyskinesias: A new subtype or variations on classic themes? [Meeting Abstract]

Pourfar, MH; Guerrini, R; Frucht, SJ
ISI:000221639600267
ISSN: 0885-3185
CID: 2763492