These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
154 related articles for article (PubMed ID: 37494148)
21. A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations. Herzog A; Hartung R; Reuser AJ; Hermanns P; Runz H; Karabul N; Gökce S; Pohlenz J; Kampmann C; Lampe C; Beck M; Mengel E Orphanet J Rare Dis; 2012 Jun; 7():35. PubMed ID: 22676651 [TBL] [Abstract][Full Text] [Related]
22. [Pompe disease treated with enzyme replacement therapy in pregnancy]. Grosz Z; Várdi KV; Molnár JM Ideggyogy Sz; 2020 Sep; 73(9-10):339-344. PubMed ID: 33035415 [TBL] [Abstract][Full Text] [Related]
23. Early-onset of symptoms and clinical course of Pompe disease associated with the c.-32-13 T > G variant. Herbert M; Case LE; Rairikar M; Cope H; Bailey L; Austin SL; Kishnani PS Mol Genet Metab; 2019 Feb; 126(2):106-116. PubMed ID: 30655185 [TBL] [Abstract][Full Text] [Related]
24. Newborn screening for Pompe disease: Parental experiences and follow-up care for a late-onset diagnosis. Prakash S; Penn JD; Jackson KE; Dean LW J Genet Couns; 2022 Dec; 31(6):1404-1420. PubMed ID: 35915971 [TBL] [Abstract][Full Text] [Related]
25. Familial Pompe Disease. Tecellioglu M; Kamisli O Med Arch; 2015 Oct; 69(5):342-4. PubMed ID: 26622091 [TBL] [Abstract][Full Text] [Related]
26. Pompe disease ascertained through The Lantern Project, 2018-2021: Next-generation sequencing and enzymatic testing to overcome obstacles to diagnosis. Sniderman King L; Pan Y; Nallamilli BRR; Hegde M; Jagannathan L; Ramachander V; Lucas A; Markind J; Colzani R Mol Genet Metab; 2023 May; 139(1):107565. PubMed ID: 37087815 [TBL] [Abstract][Full Text] [Related]
31. A Case of Adult-onset Pompe Disease with Cerebral Stroke and Left Ventricular Hypertrophy. Hossain MA; Miyajima T; Akiyama K; Eto Y J Stroke Cerebrovasc Dis; 2018 Nov; 27(11):3046-3052. PubMed ID: 30093193 [TBL] [Abstract][Full Text] [Related]
32. Comparison of recent pivotal recommendations for the diagnosis and treatment of late-onset Pompe disease using diagnostic nodes-the Pompe disease burden scale. Hundsberger T; Schoser B; Leupold D; Rösler KM; Putora PM J Neurol; 2019 Aug; 266(8):2010-2017. PubMed ID: 31104135 [TBL] [Abstract][Full Text] [Related]
34. Screening for late-onset Pompe disease in Poland. Jastrzębska A; Potulska-Chromik A; Łusakowska A; Jastrzębski M; Lipowska M; Kierdaszuk B; Kamińska A; Kostera-Pruszczyk A Acta Neurol Scand; 2019 Oct; 140(4):239-243. PubMed ID: 31125121 [TBL] [Abstract][Full Text] [Related]
35. Late-onset pompe disease in Iran: A clinical and genetic report. Nazari F; Sinaei F; Nilipour Y; Fatehi F; Streubel B; Ashrafi MR; Aryani O; Nafissi S Muscle Nerve; 2017 Jun; 55(6):835-840. PubMed ID: 27649523 [TBL] [Abstract][Full Text] [Related]
36. Spanish Pompe registry: Baseline characteristics of first 49 patients with adult onset of Pompe disease. Alonso-Pérez J; Segovia S; Domínguez-González C; Olivé M; Mendoza Grimón MD; Fernández-Torrón R; López de Munain A; Muñoz-Blanco JL; Ramos-Fransi A; Almendrote M; Illa I; Díaz-Manera J Med Clin (Barc); 2020 Feb; 154(3):80-85. PubMed ID: 31253477 [TBL] [Abstract][Full Text] [Related]
37. The new era of Pompe disease: advances in the detection, understanding of the phenotypic spectrum, pathophysiology, and management. Kishnani PS; Beckemeyer AA; Mendelsohn NJ Am J Med Genet C Semin Med Genet; 2012 Feb; 160C(1):1-7. PubMed ID: 22253049 [TBL] [Abstract][Full Text] [Related]
40. The Novel Compound Heterozygous Mutations of GAA Gene in Mainland Chinese Patient with Classic Infantile-Onset Pompe Disease. Li J; Cui Y; Wang X; Wang Q; Wang H; Yan B Int Heart J; 2020 Jan; 61(1):178-182. PubMed ID: 31875618 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]