895 related articles for article (PubMed ID: 18439925)
1. [A retrospective study of six patients with late-onset Pompe disease].
Saux A; Laforet P; Pagès AM; Figarella-Branger D; Pellissier JF; Pagès M; Labauge P
Rev Neurol (Paris); 2008 Apr; 164(4):336-42. PubMed ID: 18439925
[TBL] [Abstract][Full Text] [Related]
2. [Enzyme replacement therapy in Pompe's disease].
Merk T; Wibmer T; Schumann C; Krüger S
Med Klin (Munich); 2007 Jul; 102(7):570-3. PubMed ID: 17634875
[TBL] [Abstract][Full Text] [Related]
3. Clinical manifestation and natural course of late-onset Pompe's disease in 54 Dutch patients.
Hagemans ML; Winkel LP; Van Doorn PA; Hop WJ; Loonen MC; Reuser AJ; Van der Ploeg AT
Brain; 2005 Mar; 128(Pt 3):671-7. PubMed ID: 15659425
[TBL] [Abstract][Full Text] [Related]
4. [Adult form of Pompe disease].
Ziółkowska-Graca B; Kania A; Zwolińska G; Nizankowska-Mogilnicka E
Pneumonol Alergol Pol; 2008; 76(5):396-9. PubMed ID: 19003770
[TBL] [Abstract][Full Text] [Related]
5. [Pompe's disease. Part I: pathogenesis and clinical features].
Illés Z; Trauninger A
Ideggyogy Sz; 2009 Jul; 62(7-8):231-43. PubMed ID: 19685701
[TBL] [Abstract][Full Text] [Related]
6. Late-onset Pompe's disease.
Teener JW
Semin Neurol; 2012 Nov; 32(5):506-11. PubMed ID: 23677658
[TBL] [Abstract][Full Text] [Related]
7. Enzyme replacement therapy in late-onset Pompe's disease: a three-year follow-up.
Winkel LP; Van den Hout JM; Kamphoven JH; Disseldorp JA; Remmerswaal M; Arts WF; Loonen MC; Vulto AG; Van Doorn PA; De Jong G; Hop W; Smit GP; Shapira SK; Boer MA; van Diggelen OP; Reuser AJ; Van der Ploeg AT
Ann Neurol; 2004 Apr; 55(4):495-502. PubMed ID: 15048888
[TBL] [Abstract][Full Text] [Related]
8. Acid maltase deficiency in adults. A study of five cases.
Lenders MB; Martin JJ; de Barsy T; Ceuterick C; Marchau M
Acta Neurol Belg; 1986; 86(3):152-60. PubMed ID: 3090848
[TBL] [Abstract][Full Text] [Related]
9. [Myopathy associated with respiratory insufficiency: diagnostic difficulties in adult-onset Pompe disease].
Merkli H; Pál E; Nagy F; Horváth R; Várdi VK; Komoly S; Illés Z
Orv Hetil; 2006 Jul; 147(30):1421-4. PubMed ID: 16977780
[TBL] [Abstract][Full Text] [Related]
10. [Glycogen storage disease (Pompe's disease) presenting as myopathy in the adult (author's transl)].
Stefan H; Böker DK; Müller J; Gullotta F
Dtsch Med Wochenschr; 1977 Oct; 102(42):1512-4. PubMed ID: 269788
[TBL] [Abstract][Full Text] [Related]
11. [Late infantile form of Pompe's disease. Deficiency of alpha-1,4-glucosidase (acid maltase)].
Colomer J; Roig M; Campistol J; Rullan G; Fernández-Alvarez E
An Esp Pediatr; 1984 Sep; 21(3):250-9. PubMed ID: 6391315
[TBL] [Abstract][Full Text] [Related]
12. A randomized study of alglucosidase alfa in late-onset Pompe's disease.
van der Ploeg AT; Clemens PR; Corzo D; Escolar DM; Florence J; Groeneveld GJ; Herson S; Kishnani PS; Laforet P; Lake SL; Lange DJ; Leshner RT; Mayhew JE; Morgan C; Nozaki K; Park DJ; Pestronk A; Rosenbloom B; Skrinar A; van Capelle CI; van der Beek NA; Wasserstein M; Zivkovic SA
N Engl J Med; 2010 Apr; 362(15):1396-406. PubMed ID: 20393176
[TBL] [Abstract][Full Text] [Related]
13. Adeno-associated virus-mediated transfer of human acid maltase gene results in a transient reduction of glycogen accumulation in muscle of Japanese quail with acid maltase deficiency.
Lin CY; Ho CH; Hsieh YH; Kikuchi T
Gene Ther; 2002 May; 9(9):554-63. PubMed ID: 11973631
[TBL] [Abstract][Full Text] [Related]
14. Broad spectrum of Pompe disease in patients with the same c.-32-13T->G haplotype.
Kroos MA; Pomponio RJ; Hagemans ML; Keulemans JL; Phipps M; DeRiso M; Palmer RE; Ausems MG; Van der Beek NA; Van Diggelen OP; Halley DJ; Van der Ploeg AT; Reuser AJ
Neurology; 2007 Jan; 68(2):110-5. PubMed ID: 17210890
[TBL] [Abstract][Full Text] [Related]
15. [Clinical manifestations, course and outcome of enzyme replacement therapy in Hungarian patients with Pompe's disease].
Bereznai B; Trauninger A; György I; Szakszon K; Almássy Z; Pál E; Herczegfalvi A; Várdi Visy K; Illés Z; Molnár MJ
Orv Hetil; 2011 Sep; 152(39):1569-75. PubMed ID: 21920843
[TBL] [Abstract][Full Text] [Related]
16. Diagnostic criteria for late-onset (childhood and adult) Pompe disease.
American Association of Neuromuscular & Electrodiagnostic Medicine
Muscle Nerve; 2009 Jul; 40(1):149-60. PubMed ID: 19533647
[TBL] [Abstract][Full Text] [Related]
17. Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form.
Verloes A; Massin M; Lombet J; Grattagliano B; Soyeur D; Rigo J; Koulischer L; Van Hoof F
Am J Med Genet; 1997 Oct; 72(2):135-42. PubMed ID: 9382133
[TBL] [Abstract][Full Text] [Related]
18. Pompe disease (glycogen storage disease type II): clinical features and enzyme replacement therapy.
van der Beek NA; Hagemans ML; van der Ploeg AT; Reuser AJ; van Doorn PA
Acta Neurol Belg; 2006 Jun; 106(2):82-6. PubMed ID: 16898258
[TBL] [Abstract][Full Text] [Related]
19. Late onset Pompe disease: clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients.
Müller-Felber W; Horvath R; Gempel K; Podskarbi T; Shin Y; Pongratz D; Walter MC; Baethmann M; Schlotter-Weigel B; Lochmüller H; Schoser B
Neuromuscul Disord; 2007 Oct; 17(9-10):698-706. PubMed ID: 17643989
[TBL] [Abstract][Full Text] [Related]
20. [Three hypotonic neonates with hypertrophic cardiomyopathy: Pompe's disease].
Willemsen MA; Jira PE; Gabreëls FJ; van der Ploeg AT; Smeitink JA
Ned Tijdschr Geneeskd; 1998 Jun; 142(24):1388-92. PubMed ID: 9752027
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
