Glatzl J - Search Results

1

CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.

Geley S, Kapelari K, Jöhrer K, Peter M, Glatzl J, Vierhapper H, Schwarz S, Helmberg A, Sippell WG, White PC, Kofler R. Geley S, et al. Among authors: glatzl j. J Clin Endocrinol Metab. 1996 Aug;81(8):2896-901. doi: 10.1210/jcem.81.8.8768848. J Clin Endocrinol Metab. 1996. PMID: 8768848

2

Hereditary complete deficiency of the fourth component of complement: effects on the kidney.

Lhotta K, Thoenes W, Glatzl J, Hintner H, Kronenberg F, Joannidis M, König P. Lhotta K, et al. Among authors: glatzl j. Clin Nephrol. 1993 Mar;39(3):117-24. Clin Nephrol. 1993. PMID: 8462200

3

Androgen receptor point mutations as the underlying molecular defect in 2 patients with androgen insensitivity syndrome.

Radmayr C, Culig Z, Glatzl J, Neuschmid-Kaspar F, Bartsch G, Klocker H. Radmayr C, et al. Among authors: glatzl j. J Urol. 1997 Oct;158(4):1553-6. J Urol. 1997. PMID: 9302173

4

Characterization of two point mutations in the androgen receptor gene of patients with perineoscrotal hypospadia.

Kaspar F, Cato AC, Denninger A, Eberle J, Radmayr C, Glatzl J, Bartsch G, Klocker H. Kaspar F, et al. Among authors: glatzl j. J Steroid Biochem Mol Biol. 1993 Dec;47(1-6):127-35. doi: 10.1016/0960-0760(93)90066-6. J Steroid Biochem Mol Biol. 1993. PMID: 8274427

5

Hereditary angio-oedema: treatment with danazol. Report of a case.

Tappeiner G, Hintner H, Glatzl J, Wolff K. Tappeiner G, et al. Among authors: glatzl j. Br J Dermatol. 1979 Feb;100(2):207-12. doi: 10.1111/j.1365-2133.1979.tb05562.x. Br J Dermatol. 1979. PMID: 427020

6

Screening of patients with Turner syndrome for "hidden" Y-mosaicism.

Vlasak I, Plöchl E, Kronberger G, Bergendi E, Rittinger O, Hagemann M, Schmitt K, Blümel P, Glatzl J, Fekete G, Kadrnka-Lovrencic M, Borkenstein M, Häusler G, Frisch H. Vlasak I, et al. Among authors: glatzl j. Klin Padiatr. 1999 Jan-Feb;211(1):30-4. doi: 10.1055/s-2008-1043759. Klin Padiatr. 1999. PMID: 10067216

7

Follow-up of Ullrich's original patient with "Ullrich-Turner" syndrome.

Wiedemann HR, Glatzl J. Wiedemann HR, et al. Among authors: glatzl j. Am J Med Genet. 1991 Oct 1;41(1):134-6. doi: 10.1002/ajmg.1320410132. Am J Med Genet. 1991. PMID: 1951454

8

Neopterin levels during acute rubella in children.

Zaknun D, Weiss G, Glatzl J, Wachter H, Fuchs D. Zaknun D, et al. Among authors: glatzl j. Clin Infect Dis. 1993 Sep;17(3):521-2. doi: 10.1093/clinids/17.3.521. Clin Infect Dis. 1993. PMID: 8218709 No abstract available.

9

Precocious puberty due to a lipid-cell tumour of the ovary.

Dengg K, Fink FM, Heitger A, Tabarelli M, Kreczy A, Glatzl J, Berger H. Dengg K, et al. Among authors: glatzl j. Eur J Pediatr. 1993 Jan;152(1):12-4. doi: 10.1007/BF02072508. Eur J Pediatr. 1993. PMID: 8444198

10

[Intersexual genitals].

Glatzl J. Glatzl J. Padiatr Padol. 1991;26(3):135-41. Padiatr Padol. 1991. PMID: 1945475 Review. German.

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