Bonfig W - Search Results

1

Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndrome.

Bonfig W, Salem NJ, Heiliger K, Hempel M, Lederer G, Bornkamm M, Wieland K, Lohse P, Burdach S, Oexle K. Bonfig W, et al. J Pediatr Endocrinol Metab. 2012;25(9-10):991-5. doi: 10.1515/jpem-2012-0103. J Pediatr Endocrinol Metab. 2012. PMID: 23426831

2

Pubertal height gain in Ullrich-Turner syndrome.

Bechtold S, Dalla Pozza R, Schmidt H, Bonfig W, Schwarz HP. Bechtold S, et al. Among authors: bonfig w. J Pediatr Endocrinol Metab. 2006 Aug;19(8):987-93. doi: 10.1515/jpem.2006.19.8.987. J Pediatr Endocrinol Metab. 2006. PMID: 16995583

3

Reassessment of the optimal growth hormone cut-off level in insulin tolerance testing for growth hormone secretion in patients with childhood-onset growth hormone deficiency during transition to adulthood.

Bonfig W, Bechtold S, Bachmann S, Putzker S, Fuchs O, Pagel P, Schwarz HP. Bonfig W, et al. J Pediatr Endocrinol Metab. 2008 Nov;21(11):1049-56. doi: 10.1515/jpem.2008.21.11.1049. J Pediatr Endocrinol Metab. 2008. PMID: 19189699

4

GCK-MODY (MODY 2) Caused by a Novel p.Phe330Ser Mutation.

Bonfig W, Hermanns S, Warncke K, Eder G, Engelsberger I, Burdach S, Ziegler AG, Lohse P. Bonfig W, et al. ISRN Pediatr. 2011;2011:676549. doi: 10.5402/2011/676549. Epub 2011 Apr 26. ISRN Pediatr. 2011. PMID: 22389783 Free PMC article.

5

Avoiding harmful procedures in patients with elevated α-fetoprotein concentrations: hereditary persistence of α-fetoprotein is an important and benign differential diagnosis!

Bonfig W, Hempel M, Teichert-von Lüttichau I, Liptay S, Burdach S. Bonfig W, et al. J Pediatr Hematol Oncol. 2012 Oct;34(7):e301-3. doi: 10.1097/MPH.0b013e3182441256. J Pediatr Hematol Oncol. 2012. PMID: 22430587

6

Severe pretreatment cerebral edema in newly diagnosed type 1 diabetes.

Warncke K, Dressel P, Ziegler AG, Steinborn M, Bonfig W, Burdach S, Engelsberger I. Warncke K, et al. Among authors: bonfig w. Horm Res Paediatr. 2014;81(4):285-8. doi: 10.1159/000357140. Epub 2014 Mar 13. Horm Res Paediatr. 2014. PMID: 24642459

7

Genetic characteristics and long-term follow-up of 11 patients with congenital hyperinsulinism followed in a single center.

Warncke K, Falco F, Rabl W, Engelsberger I, Saier J, Flores-Rodriguez D, Burdach S, Bonfig W. Warncke K, et al. Among authors: bonfig w. J Pediatr Endocrinol Metab. 2016 Oct 1;29(10):1187-1194. doi: 10.1515/jpem-2016-0103. J Pediatr Endocrinol Metab. 2016. PMID: 27682711 Clinical Trial.

8

Recurrent hypoglycemic seizures and obesity: delayed diagnosis of an insulinoma in a 15 year-old boy--final diagnostic localization with endosonography.

Bonfig W, Kann P, Rothmund M, Schwarz HP. Bonfig W, et al. J Pediatr Endocrinol Metab. 2007 Sep;20(9):1035-8. doi: 10.1515/jpem.2007.20.9.1035. J Pediatr Endocrinol Metab. 2007. PMID: 18038712

9

Successful early dietary intervention avoids obesity in patients with Prader-Willi syndrome: a ten-year follow-up.

Schmidt H, Pozza SB, Bonfig W, Schwarz HP, Dokoupil K. Schmidt H, et al. Among authors: bonfig w. J Pediatr Endocrinol Metab. 2008 Jul;21(7):651-5. doi: 10.1515/JPEM.2008.21.7.651. J Pediatr Endocrinol Metab. 2008. PMID: 18780599

10

Overestimation of final height prediction in patients with classical congenital adrenal hyperplasia using the Bayley and Pinneau method.

Bonfig W, Schwarz HP. Bonfig W, et al. J Pediatr Endocrinol Metab. 2012;25(7-8):645-9. doi: 10.1515/jpem-2012-0122. J Pediatr Endocrinol Metab. 2012. PMID: 23155688

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