Searched for: in-biosketch:true
person:kruppl01
Retrospective analysis of rituximab treatment of 24 cases of neuromyelitis optica [Meeting Abstract]
Jacob, Anu; Weinshenker, Brian; McLinskey, Nancy; Krupp, Lauren; Ivo, Violich; Fox, Robert; Boggild, Mike; Matiello, Marcelo; Wingerchuk, Dean; Cree, Bruce
ISI:000245175001310
ISSN: 0028-3878
CID: 2233222
Neuroprogenitor cell detection in patients with multiple sclerosis [Meeting Abstract]
Savatic, Mirjana; Li, Haifang; Li, Yao; Djuric, Petar; Krupp, Lauren
ISI:000249930600283
ISSN: 0364-5134
CID: 2233432
Clinical spectrum of diagnoses in children referred for evaluation of acquired CNS demyelinating disorders including pediatric multiple sclerosis [Meeting Abstract]
Belman, A; Chabas, D; Chitnis, T; Gorman, M; Weinstock-Guttman, B; Kuntz, N; Krupp, L; McLinskey, N; Ness, J; Rodriguez, M; Waubant, E; Yeh, A
ISI:000249930600388
ISSN: 0364-5134
CID: 2233442
Validation of consistent improvement in walking speed on the Timed 25 Foot Walk as a measure of clinically meaningful change [Meeting Abstract]
Goodman, AD; Brown, TR; Cohen, JA; Krupp, L; Schapiro, R; Schwid, SR; Cohen, R; Marinucci, L; Blight, A
ISI:000251447300074
ISSN: 1352-4585
CID: 2234042
Longitudinal patterns of fatigue in patients with multiple sclerosis [Meeting Abstract]
Lerdal, A; Cellos, EG; Krupp, L; Dahl, A
ISI:000251423400345
ISSN: 1352-4585
CID: 2234262
Earlier age at onset is related to lower education level in male patients with multiple sclerosis [Meeting Abstract]
Teter, BE; Weinstock-Guttman, B; Apatoff, B; Blitz, K; Christodoulou, C; Coyle, PK; Frontera, A; Goodman, A; Gottesman, MH; Granger, Cy; Herbert, J; Holub, R; Jubelt, B; Kahn, M; Krupp, L; Munschauer, F., III; Lava, N; Lenihan, M; Lublin, F; Mihai, C; Miller, AE; Perel, A; Schwid, S; Smiroldo, J; Snyder, DH; Zivadinov, R; Tullman, M
ISI:000251423400351
ISSN: 1352-4585
CID: 2234272
Meta-analysis of Phase 2 and 3 Fampridine Trials in Multiple Sclerosis: efficacy assessment and validation of clinical meaningfulness of outcome measure [Meeting Abstract]
Goodman, AD; Brown, TR; Cohen, JA; Krupp, L; Schapiro, R; Schwid, SR; Cohen, R; Marinucci, L; Blight, A
ISI:000251423400082
ISSN: 1352-4585
CID: 2234382
Pediatric multiple sclerosis and related disorders
Krupp, Lauren B; Hertz, Deborah P
Hagerstown, MD : Lippincott Williams & Wilkins, 2007
Extent: 74 p. ; 28 cm.
ISBN: n/a
CID: 2234532
Fatigue in multiple sclerosis
Chapter by: Krupp, Lauren; McLinskey, N; MacAllister, W
in: Multiple sclerosis therapeutics by Cohen, Jeffrey Alan; Rudick, Richard A [Eds]
Abingdon : Informa Healthcare, 2007
pp. 733-786
ISBN: 1841845256
CID: 2235952
High-dose cyclophosphamide for moderate to severe refractory multiple sclerosis
Gladstone, Douglas E; Zamkoff, Kenneth W; Krupp, Lauren; Peyster, Robert; Sibony, Patrick; Christodoulou, Christopher; Locher, Emily; Coyle, Patricia K
BACKGROUND: High-dose cyclophosphamide is active in immune-mediated illnesses. OBJECTIVE: To describe the effects of high-dose cyclophosphamide on severe refractory multiple sclerosis. DESIGN, SETTING, AND PATIENTS: Patients with multiple sclerosis with an Expanded Disability Status Scale (EDSS) score of 3.5 or higher after 2 or more Food and Drug Administration-approved disease-modifying therapy regimens were evaluated. INTERVENTIONS: Patients received 200 mg/kg of cyclophosphamide over 4 days. MAIN OUTCOME MEASURES: Patients had brain magnetic resonance imaging and neuro-ophthalmologic evaluations every 6 months and quarterly EDSS and quality-of-life evaluations for 2 years. RESULTS: Twelve patients were evaluated for clinical response (median follow-up, 15.0 months; follow-up range, 6-24 months). During follow-up, no patients increased their baseline EDSS scores by more than 1.0. Five patients decreased their EDSS scores by 1.0 or more (EDSS score decrease range, 1.0-5.0). Two of 11 patients had a single enhancing lesion at baseline; these lesions resolved after high-dose cyclophosphamide treatment. At 12 months, 1 patient showed 1 new enhancing lesion without a corresponding high-intensity T2-weighted or fluid-attenuated inversion recovery signal. Patients reported improvement in all of the quality-of-life parameters measured. Neurologic improvement involved changes in gait, bladder control, and visual function. Treatment response was seen regardless of the baseline presence or absence of contrast lesion activity. Patient quality-of-life improvement occurred independently of EDSS score changes. In this small group of patients with treatment-refractory multiple sclerosis, high-dose cyclophosphamide was associated with minimal morbidity and improved clinical outcomes. CONCLUSIONS: High-dose cyclophosphamide treatment in patients with severe refractory multiple sclerosis can result in disease stabilization, improved functionality, and improved quality of life. Further studies are necessary to determine the most appropriate patients for this treatment.
PMID: 16908728
ISSN: 0003-9942
CID: 2153702