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1.
Establishing how much improvement in lung function and distance walked is clinically important for adult patients with Pompe disease.
Eur J Neurol
; 31(5): e16223, 2024 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-38375606
2.
Neurofilament light protein as a biomarker for spinal muscular atrophy: a review and reference ranges.
Clin Chem Lab Med
; 62(7): 1252-1265, 2024 Jun 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-38215341
3.
Association between changes in pulmonary function and in patient reported outcomes during enzyme therapy of adult patients with late-onset Pompe disease.
J Inherit Metab Dis
; 46(4): 595-604, 2023 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-36966448
4.
Lysosomal glycogen accumulation in Pompe disease results in disturbed cytoplasmic glycogen metabolism.
J Inherit Metab Dis
; 46(1): 101-115, 2023 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-36111639
5.
Effect of Anti-Iduronate 2-Sulfatase Antibodies in Patients with Mucopolysaccharidosis Type II Treated with Enzyme Replacement Therapy.
J Pediatr
; 248: 100-107.e3, 2022 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-35568060
6.
MRI changes in diaphragmatic motion and curvature in Pompe disease over time.
Eur Radiol
; 32(12): 8681-8691, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-35829785
7.
Is the brain involved in patients with late-onset Pompe disease?
J Inherit Metab Dis
; 45(3): 493-501, 2022 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-34927739
8.
Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway.
J Inherit Metab Dis
; 45(5): 952-962, 2022 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-35722880
9.
Update of the Pompe variant database for the prediction of clinical phenotypes: Novel disease-associated variants, common sequence variants, and results from newborn screening.
Hum Mutat
; 42(2): 119-134, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33560568
10.
Broad variation in phenotypes for common GAA genotypes in Pompe disease.
Hum Mutat
; 42(11): 1461-1472, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34405923
11.
Can serial cerebral MRIs predict the neuronopathic phenotype of MPS II?
J Inherit Metab Dis
; 44(3): 751-762, 2021 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33330992
12.
Prenatal Enzyme-Replacement Therapy.
N Engl J Med
; 387(23): 2189-2193, 2022 12 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-36351269
13.
Effects of higher and more frequent dosing of alglucosidase alfa and immunomodulation on long-term clinical outcome of classic infantile Pompe patients.
J Inherit Metab Dis
; 43(6): 1243-1253, 2020 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-32506446
14.
Retrospective evaluation of the Dutch pre-newborn screening cohort for propionic acidemia and isolated methylmalonic acidemia: What to aim, expect, and evaluate from newborn screening?
J Inherit Metab Dis
; 43(3): 424-437, 2020 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-31828787
15.
GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry.
Hum Mutat
; 40(11): 2146-2164, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31342611
16.
Extension of the Pompe mutation database by linking disease-associated variants to clinical severity.
Hum Mutat
; 40(11): 1954-1967, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31254424
17.
The lysosomal storage disorders mucolipidosis type II, type III alpha/beta, and type III gamma: Update on GNPTAB and GNPTG mutations.
Hum Mutat
; 40(7): 842-864, 2019 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-30882951
18.
microRNAs as biomarkers in Pompe disease.
Genet Med
; 21(3): 591-600, 2019 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29997386
19.
Decreased plasma l-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment.
Mol Genet Metab
; 126(4): 397-405, 2019 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30827756
20.
Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry.
J Inherit Metab Dis
; 42(6): 1162-1175, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-30734935