Clinical features of late-onset Pompe disease: ... [Muscle Nerve. 2008] - PubMed

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Rate of disease progression during long-term follow-up of patients with late-onset Pompe disease. [Neuromuscul Disord. 2009]
Rate of disease progression during long-term follow-up of patients with late-onset Pompe disease.
Van der Beek NA, Hagemans ML, Reuser AJ, Hop WC, Van der Ploeg AT, Van Doorn PA, Wokke JH. Neuromuscul Disord. 2009 Feb; 19(2):113-7. Epub 2008 Dec 11.
Use of the muscle volume analyzer to evaluate enzyme replacement therapy in late-onset Pompe disease. [J Neurol. 2010]
Use of the muscle volume analyzer to evaluate enzyme replacement therapy in late-onset Pompe disease.
Sugai F, Kokunai Y, Yamamoto Y, Hashida G, Shimazu K, Mihara M, Inoue S, Sakoda S. J Neurol. 2010 Mar; 257(3):461-3. Epub 2009 Nov 12.
Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS. [Neurology. 2009]
Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS.
Gordon PH, Cheng B, Katz IB, Mitsumoto H, Rowland LP. Neurology. 2009 Jun 2; 72(22):1948-52.
Review Physical therapy management of Pompe disease. [Genet Med. 2006]
Review Physical therapy management of Pompe disease.
Case LE, Kishnani PS. Genet Med. 2006 May; 8(5):318-27.
Review Pompe disease: a neuromuscular disease with respiratory muscle involvement. [Respir Med. 2009]
Review Pompe disease: a neuromuscular disease with respiratory muscle involvement.
Mellies U, Lofaso F. Respir Med. 2009 Apr; 103(4):477-84. Epub 2009 Jan 7.

Hearing in adults with Pompe disease. [J Inherit Metab Dis. 2012]
Hearing in adults with Pompe disease.
van der Beek NA, Verschuure H, Reuser AJ, van der Ploeg AT, van Doorn PA, Poublon RM. J Inherit Metab Dis. 2012 Mar; 35(2):335-41. Epub 2011 Oct 15.
Cardiovascular abnormalities in late-onset Pompe disease and response to enzyme replacement therapy. [Genet Med. 2011]
Cardiovascular abnormalities in late-onset Pompe disease and response to enzyme replacement therapy.
Forsha D, Li JS, Smith PB, van der Ploeg AT, Kishnani P, Pasquali SK, Late-Onset Treatment Study Investigators. Genet Med. 2011 Jul; 13(7):625-31.
Progress in Enzyme Replacement Therapy in Glycogen Storage Disease Type II. [Ther Adv Neurol Disord. 2009]
Progress in Enzyme Replacement Therapy in Glycogen Storage Disease Type II.
Angelini C, Semplicini C, Tonin P, Filosto M, Pegoraro E, Sorarù G, Fanin M. Ther Adv Neurol Disord. 2009 May; 2(3):143-53.

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Clinical features of late-onset Pompe disease: a prospective cohort study.
Clinical features of late-onset Pompe disease: a prospective cohort study.
Muscle Nerve. 2008 Oct ;38(4):1236-45.

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