J G Langendonk
Overview
Explore the profile of J G Langendonk including associated specialties, affiliations and a list of published articles.
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Articles
17
Citations
248
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0
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Recent Articles
1.
Timmer C, Davids M, Nieuwdorp M, Levels J, Langendonk J, Breederveld M, et al.
Mol Genet Metab Rep
. 2021 Sep;
29:100794.
PMID: 34527515
Take Home Message: The faecal microbiome of UCD patients was less diverse compared to PKU patients and even more compared to healthy controls.
2.
Wensink D, Langendonk J, Overbey J, Balwani M, Van Broekhoven E, Wagenmakers M, et al.
Genet Med
. 2021 May;
23(9):1616-1623.
PMID: 33941881
Purpose: Patients with erythropoietic protoporphyria (EPP), a severe painful photodermatosis, experience prodromal sensations when exposed to sunlight, which are the "warning signals" to exit the sun, as prolonged exposure causes...
3.
Molema F, Haijes H, Janssen M, Bosch A, van Spronsen F, Mulder M, et al.
Clin Nutr
. 2021 Jan;
40(5):3622-3630.
PMID: 33451859
Background And Objective: Methylmalonic acidemia (MMA) and propionic acidemia (PA) are inborn errors of metabolism. While survival of MMA and PA patients has improved in recent decades, long-term outcome is...
4.
Neeleman R, Wensink D, Wagenmakers M, Mijnhout G, Friesema E, Langendonk J
Neth J Med
. 2020 Jul;
78(4):149-160.
PMID: 32641543
Porphyrias are rare metabolic disorders. Lack of awareness and knowledge about the clinical features of porphyrias results in diagnostic and therapeutic delays for many patients. Delays in diagnosing and treating...
5.
Rubio-Gozalbo M, Haskovic M, Bosch A, Burnyte B, Coelho A, Cassiman D, et al.
Orphanet J Rare Dis
. 2019 Apr;
14(1):86.
PMID: 31029175
Background: Classic galactosemia is a rare inborn error of carbohydrate metabolism, caused by a severe deficiency of the enzyme galactose-1-phosphate uridylyltransferase (GALT). A galactose-restricted diet has proven to be very...
6.
Molema F, Jacobs E, Onkenhout W, Schoonderwoerd G, Langendonk J, Williams M
J Inherit Metab Dis
. 2018 Aug;
41(6):1179-1187.
PMID: 30159853
Background: There is increasing evidence that long-term complications in organic acidemias are caused by impaired mitochondrial metabolism. Currently, there is no specific biomarker to monitor mitochondrial dysfunction in organic acidemias....
7.
Suijker I, Savas M, van Rossum E, Langendonk J
Br J Dermatol
. 2018 Jan;
178(5):1209-1210.
PMID: 29341104
No abstract available.
8.
Biewenga M, Matawlie R, Friesema E, Koole-Lesuis H, Langeveld M, Wilson J, et al.
Br J Dermatol
. 2017 Aug;
177(6):1693-1698.
PMID: 28815553
Background: Erythropoietic protoporphyria (EPP) is a rare metabolic disease with painful photosensitivity due to protoporphyrin IX accumulation. Objectives: To evaluate bone mineral density (BMD) and known osteoporosis risk factors in...
9.
Rutten M, Ciet P, Biggelaar R, Oussoren E, Langendonk J, van der Ploeg A, et al.
Orphanet J Rare Dis
. 2016 Apr;
11:50.
PMID: 27112191
Background: Mucopolysaccharidosis type II (MPSII) patients frequently suffer from dyspnoea caused by restrictive airway disease due to skeletal abnormalities as well as glycosaminoglycans (GAG) accumulation at different levels of the...
10.