Whitaker C - Search Results

1

Multicenter expanded access program for access to investigational products for amyotrophic lateral sclerosis.

Neel DV, Baselga-Garriga C, Benson M, Keegan M, Chase M, D'Agostino D, Drake K, Hagar JL, Hasenoehrl MG, Kulesa-Kelley J, Leite A, Mohapatra S, Portaro SM, Pothier LM, Rosenthal J, Sherman AV, Yu H, McCaffrey A, Ho D, Luppino S, Bedlack R, Heitzman D, Ajroud-Driss S, Katz J, Felice K, Whitaker C, Ladha S, Alameda G, Locatelli E, Qureshi IA, Hotchkin MT, Hayden MR, Cudkowicz ME, Babu S, Berry JD, Paganoni S. Neel DV, et al. Among authors: whitaker c. Muscle Nerve. 2024 Aug;70(2):232-239. doi: 10.1002/mus.28169. Epub 2024 Jun 6. Muscle Nerve. 2024. PMID: 38842106

2

Late-onset facioscapulohumeral muscular dystrophy type 1 in previously undiagnosed families: Presenting clinical features in an often-misdiagnosed disorder.

Felice KJ, Whitaker CH. Felice KJ, et al. Muscle Nerve. 2023 Nov;68(5):758-762. doi: 10.1002/mus.27962. Epub 2023 Aug 28. Muscle Nerve. 2023. PMID: 37638785

3

Apparent conduction block in patients with ulnar neuropathy at the elbow and proximal Martin-Gruber anastomosis.

Whitaker CH, Felice KJ. Whitaker CH, et al. Muscle Nerve. 2004 Dec;30(6):808-11. doi: 10.1002/mus.20128. Muscle Nerve. 2004. PMID: 15316981

4

Fulminant lipid storage myopathy due to multiple acyl-coenzyme a dehydrogenase deficiency.

Whitaker CH, Felice KJ, Silvers D, Wu Q. Whitaker CH, et al. Muscle Nerve. 2015 Aug;52(2):289-93. doi: 10.1002/mus.24552. Epub 2015 Feb 11. Muscle Nerve. 2015. PMID: 25556768

5

Diagnostic yield of advanced genetic testing in patients with hereditary neuropathies: A retrospective single-site study.

Felice KJ, Whitaker CH, Khorasanizadeh S. Felice KJ, et al. Muscle Nerve. 2021 Oct;64(4):454-461. doi: 10.1002/mus.27368. Epub 2021 Jul 20. Muscle Nerve. 2021. PMID: 34232518

6

Adaptive Platform Trials to Transform Amyotrophic Lateral Sclerosis Therapy Development.

Paganoni S, Berry JD, Quintana M, Macklin E, Saville BR, Detry MA, Chase M, Sherman AV, Yu H, Drake K, Andrews J, Shefner J, Chibnik LB, Vestrucci M, Cudkowicz ME; Healey ALS Platform Trial Study Group. Paganoni S, et al. Ann Neurol. 2022 Feb;91(2):165-175. doi: 10.1002/ana.26285. Epub 2022 Jan 10. Ann Neurol. 2022. PMID: 34935174 Review.

7

Design and Statistical Innovations in a Platform Trial for Amyotrophic Lateral Sclerosis.

Quintana M, Saville BR, Vestrucci M, Detry MA, Chibnik L, Shefner J, Berry JD, Chase M, Andrews J, Sherman AV, Yu H, Drake K, Cudkowicz M, Paganoni S, Macklin EA; HEALEY ALS Platform Trial Study Group. Quintana M, et al. Ann Neurol. 2023 Sep;94(3):547-560. doi: 10.1002/ana.26714. Epub 2023 Jun 22. Ann Neurol. 2023. PMID: 37245090

8

Biopsy-proven alpha-glucosidase deficiency with normal lymphocyte enzyme activity.

Whitaker CH, Felice KJ, Natowicz M. Whitaker CH, et al. Muscle Nerve. 2004 Mar;29(3):440-2. doi: 10.1002/mus.10555. Muscle Nerve. 2004. PMID: 14981745

9

Myotonic Muscular Dystrophy Type 2 in CT, USA: A Single-Center Experience With 50 Patients.

Roy B, Wu Q, Whitaker CH, Felice KJ. Roy B, et al. J Clin Neuromuscul Dis. 2021 Mar 1;22(3):135-146. doi: 10.1097/CND.0000000000000340. J Clin Neuromuscul Dis. 2021. PMID: 33595997

10

Whole exome sequencing discloses a pathogenic MTM1 gene mutation and ends the diagnostic odyssey in an older woman with a progressive and seemingly sporadic myopathy: Case report and literature review of MTM1 manifesting female carriers.

Felice KJ, Whitaker CH, Wu Q. Felice KJ, et al. Neuromuscul Disord. 2018 Apr;28(4):339-345. doi: 10.1016/j.nmd.2018.02.002. Epub 2018 Feb 8. Neuromuscul Disord. 2018. PMID: 29567349 Review.

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