Markus Bettendorf
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Explore the profile of Markus Bettendorf including associated specialties, affiliations and a list of published articles.
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70
Citations
468
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Recent Articles
11.
Matejek N, Hoos J, Holterhus P, Bettendorf M, Choukair D
J Med Case Rep
. 2022 Dec;
16(1):455.
PMID: 36476353
Background: Iatrogenic Cushing's syndrome induced by oral and parenteral glucocorticoid administration is a well-known complication. Immediate withdrawal from exogenous steroids can lead to life-threatening adrenal insufficiency. However, Cushing's syndrome caused...
12.
Vogt P, Besikoglu B, Bettendorf M, Frank-Herrmann P, Zimmer J, Bender U, et al.
Syst Biol Reprod Med
. 2022 Apr;
68(4):247-257.
PMID: 35481403
")," individuals with rearranged Y chromosome breaks in their 46,XY cells are reported with male and female gender phenotypes and differences in germ cell tumour (GCT) risk. This raised the...
13.
Choukair D, Huckmann A, Mittnacht J, Breil T, Schenk J, Alrajab A, et al.
Indian J Pediatr
. 2022 Feb;
89(7):692-698.
PMID: 35103904
Objectives: To validate adult height predictions (BX) using automated and Greulich-Pyle bone age determinations in children with chronic endocrine diseases. Methods: Heights and near-adult heights were measured in 82 patients...
14.
Vick P, Eberle B, Choukair D, Weiss B, Roeth R, Schneider I, et al.
Genes (Basel)
. 2021 Dec;
12(12).
PMID: 34946811
Congenital primary hypothyroidism (CH; OMIM 218700) is characterized by an impaired thyroid development, or dyshormonogenesis, and can lead to intellectual disability and growth retardation if untreated. Most of the children...
15.
Gohlke B, Bettendorf M, Binder G, Hauffa B, Reinehr T, Dorr H, et al.
Klin Padiatr
. 2021 Dec;
234(2):61-67.
PMID: 34902873
Background: Genes, hormones and factors such as nutrition and psychosocial environment affect growth. Objective: What is the significance of various psychosocial factors on growth? Methods: Evaluation of results of a...
16.
Choukair D, Hauck F, Bettendorf M, Krude H, Klein C, Baumer T, et al.
Orphanet J Rare Dis
. 2021 Nov;
16(1):474.
PMID: 34772435
Background: Diagnosis, treatment, and care of patients with rare diseases require multidisciplinary cooperation between medical and paramedical specialities and with patients and families. Innovative genetic diagnostics, whole exome and whole...
17.
Hoyer-Kuhn H, Huebner A, Richter-Unruh A, Bettendorf M, Rohrer T, Kapelari K, et al.
Endocr Connect
. 2021 Apr;
10(5):561-569.
PMID: 33909597
Objective: Treatment of classic congenital adrenal hyperplasia (CAH) is necessary to compensate for glucocorticoid/mineralocorticoid deficiencies and to suppress androgen excess. Hydrocortisone (HC) is preferred in growing children with classic CAH...
18.
Lucas-Herald A, Bryce J, Kyriakou A, Ljubicic M, Arlt W, Audi L, et al.
Eur J Endocrinol
. 2021 Mar;
184(6):791-801.
PMID: 33780351
Objectives: To determine trends in clinical practice for individuals with DSD requiring gonadectomy. Design: Retrospective cohort study. Methods: Information regarding age at gonadectomy according to diagnosis; reported sex; time of...
19.
Matejek N, Tittel S, Haberland H, Rohrer T, Busemann E, Jorch N, et al.
Eur J Pediatr
. 2021 Mar;
180(8):2401-2408.
PMID: 33768331
Neonatal screening for congenital primary hypothyroidism (CH) may not distinguish between transient (TCH) and permanent dysfunction (PCH), causing potential overtreatment and concerns in affected families. To specify the indication for...
20.
Thomann J, Tittel S, Voss E, Oeverink R, Palm K, Fricke-Otto S, et al.
Int J Neonatal Screen
. 2021 Mar;
7(1).
PMID: 33673307
Neonatal screening for congenital primary hypothyroidism (CH) is mandatory in Germany but medical care thereafter remains inconsistent. Therefore, the registry HypoDok of the German Society of Pediatric Endocrinology and Diabetology...