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Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey.
Raue F, Pichl J, Dörr HG, Schnabel D, Heidemann P, Hammersen G, Jaursch-Hancke C, Santen R, Schöfl C, Wabitsch M, Haag C, Schulze E, Frank-Raue K. Raue F, et al. Among authors: wabitsch m. Clin Endocrinol (Oxf). 2011 Dec;75(6):760-5. doi: 10.1111/j.1365-2265.2011.04142.x. Clin Endocrinol (Oxf). 2011. PMID: 21645025
Efficacy and safety of setmelanotide, an MC4R agonist, in individuals with severe obesity due to LEPR or POMC deficiency: single-arm, open-label, multicentre, phase 3 trials.
Clément K, van den Akker E, Argente J, Bahm A, Chung WK, Connors H, De Waele K, Farooqi IS, Gonneau-Lejeune J, Gordon G, Kohlsdorf K, Poitou C, Puder L, Swain J, Stewart M, Yuan G, Wabitsch M, Kühnen P; Setmelanotide POMC and LEPR Phase 3 Trial Investigators. Clément K, et al. Among authors: wabitsch m. Lancet Diabetes Endocrinol. 2020 Dec;8(12):960-970. doi: 10.1016/S2213-8587(20)30364-8. Epub 2020 Oct 30. Lancet Diabetes Endocrinol. 2020. PMID: 33137293 Clinical Trial.
Novel homozygous AIRE mutation in a German patient with severe APECED.
von Schnurbein J, Lahr G, Posovszky C, Debatin KM, Wabitsch M. von Schnurbein J, et al. Among authors: wabitsch m. J Pediatr Endocrinol Metab. 2008 Oct;21(10):1003-9. doi: 10.1515/jpem.2008.21.10.1003. J Pediatr Endocrinol Metab. 2008. PMID: 19209622
A new missense mutation in the leptin gene causes mild obesity and hypogonadism without affecting T cell responsiveness.
Fischer-Posovszky P, von Schnurbein J, Moepps B, Lahr G, Strauss G, Barth TF, Kassubek J, Mühleder H, Möller P, Debatin KM, Gierschik P, Wabitsch M. Fischer-Posovszky P, et al. Among authors: wabitsch m. J Clin Endocrinol Metab. 2010 Jun;95(6):2836-40. doi: 10.1210/jc.2009-2466. Epub 2010 Apr 9. J Clin Endocrinol Metab. 2010. PMID: 20382689
The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline.
Brown RJ, Araujo-Vilar D, Cheung PT, Dunger D, Garg A, Jack M, Mungai L, Oral EA, Patni N, Rother KI, von Schnurbein J, Sorkina E, Stanley T, Vigouroux C, Wabitsch M, Williams R, Yorifuji T. Brown RJ, et al. Among authors: wabitsch m. J Clin Endocrinol Metab. 2016 Dec;101(12):4500-4511. doi: 10.1210/jc.2016-2466. Epub 2016 Oct 6. J Clin Endocrinol Metab. 2016. PMID: 27710244 Free PMC article. Review.
Vitamin D supplementation after the second year of life: joint position of the Committee on Nutrition, German Society for Pediatric and Adolescent Medicine (DGKJ e.V.), and the German Society for Pediatric Endocrinology and Diabetology (DGKED e.V.).
Reinehr T, Schnabel D, Wabitsch M, Bechtold-Dalla Pozza S, Bührer C, Heidtmann B, Jochum F, Kauth T, Körner A, Mihatsch W, Prell C, Rudloff S, Tittel B, Woelfle J, Zimmer KP, Koletzko B. Reinehr T, et al. Among authors: wabitsch m. Mol Cell Pediatr. 2019 May 6;6(1):3. doi: 10.1186/s40348-019-0090-0. Mol Cell Pediatr. 2019. PMID: 31062205 Free PMC article.
Relative leptin deficiency in children with severe early-onset obesity (SEOO) - results of the Early-onset Obesity and Leptin - German-Polish Study (EOL-GPS).
Zachurzok A, Ranke MB, Flehmig B, Jakubek-Kipa K, Marcinkiewicz K, Mazur A, Petriczko E, Pridzun L, von Schnurbein J, Walczak M, Malecka-Tendera E, Wabitsch M, Brandt S. Zachurzok A, et al. Among authors: wabitsch m. J Pediatr Endocrinol Metab. 2020 Feb 25;33(2):255-263. doi: 10.1515/jpem-2019-0469. J Pediatr Endocrinol Metab. 2020. PMID: 31927523
450 results