Dotzenrath C - Search Results

1

Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism.

Farnebo F, Teh BT, Dotzenrath C, Wassif WS, Svensson A, White I, Betz R, Goretzki P, Sandelin K, Farnebo LO, Larsson C. Farnebo F, et al. Among authors: dotzenrath c. Hum Genet. 1997 Mar;99(3):342-9. doi: 10.1007/s004390050369. Hum Genet. 1997. PMID: 9050920

2

Allelic loss of the retinoblastoma tumor suppressor gene: a marker for aggressive parathyroid tumors?

Dotzenrath C, Teh BT, Farnebo F, Cupisti K, Svensson A, Toell A, Goretzki P, Larsson C. Dotzenrath C, et al. J Clin Endocrinol Metab. 1996 Sep;81(9):3194-6. doi: 10.1210/jcem.81.9.8784068. J Clin Endocrinol Metab. 1996. PMID: 8784068

3

Molecular genetics of primary and secondary hyperparathyroidism.

Dotzenrath C, Goretzki PE, Farnebo F, Teh BT, Weber G, Röher HD, Larsson C. Dotzenrath C, et al. Exp Clin Endocrinol Diabetes. 1996;104 Suppl 4:105-7. doi: 10.1055/s-0029-1211714. Exp Clin Endocrinol Diabetes. 1996. PMID: 8981014 Review.

4

Management of primary hyperparathyroidism caused by multiple gland disease.

Goretzki PE, Dotzenrath C, Roeher HD. Goretzki PE, et al. Among authors: dotzenrath c. World J Surg. 1991 Nov-Dec;15(6):693-7. doi: 10.1007/BF01665302. World J Surg. 1991. PMID: 1685044

5

[Surgical strategy in persistence and recurrence in surgery of primary hyperparathyroidism].

Dotzenrath C, Goretzki PE, Röher HD. Dotzenrath C, et al. Langenbecks Arch Chir. 1994;379(4):218-23. doi: 10.1007/BF00186361. Langenbecks Arch Chir. 1994. PMID: 7934579 German.

6

[Reinterventions for hyperparathyroidism in multiple endocrine adenopathy].

Röher HD, Goretzki PE, Dotzenrath C. Röher HD, et al. Among authors: dotzenrath c. Wien Klin Wochenschr. 1988 May 27;100(11):364-6. Wien Klin Wochenschr. 1988. PMID: 2900582 German.

7

[Surgical therapy of secondary hyperparathyroidism after kidney transplantation].

Dotzenrath C, Goretzki PE, Röher HD. Dotzenrath C, et al. Langenbecks Arch Chir. 1993;378(2):121-4. doi: 10.1007/BF00202121. Langenbecks Arch Chir. 1993. PMID: 8474295 German.

8

Lack of MEN1 gene mutations in 27 sporadic insulinomas.

Cupisti K, Höppner W, Dotzenrath C, Simon D, Berndt I, Röher HD, Goretzki PE. Cupisti K, et al. Among authors: dotzenrath c. Eur J Clin Invest. 2000 Apr;30(4):325-9. doi: 10.1046/j.1365-2362.2000.00620.x. Eur J Clin Invest. 2000. PMID: 10759881

9

[Acute pancreatitis as the initial manifestation of primary hyperparathyroidism in children].

Dotzenrath C, Raunest J, Goretzki PE, Schmitt-Gräff A, Röher HD. Dotzenrath C, et al. Chirurg. 1990 Apr;61(4):329-30. Chirurg. 1990. PMID: 2347271 German. No abstract available.

10

[Acute abdomen in unrecognized hyperparathyroidism].

Goretzki PE, Becker H, Dotzenrath C, Grussendorf M, Röher HD. Goretzki PE, et al. Among authors: dotzenrath c. Wien Klin Wochenschr. 1988 May 27;100(11):373-5. Wien Klin Wochenschr. 1988. PMID: 3407198 German.

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