Judit Tőke - Search Results

Year	Number of Results
2002	1
2005	1
2006	2
2007	3
2008	2
2009	5
2011	1
2014	3
2015	1
2018	2
2019	1
2020	1
2021	5
2022	3
2023	4
2024	4

1

[Diagnosis of adrenocortical carcinoma].

Tőke J, Tóth M. Tőke J, et al. Orv Hetil. 2024 Jan 28;165(4):123-131. doi: 10.1556/650.2024.32958. Print 2024 Jan 28. Orv Hetil. 2024. PMID: 38281194 Hungarian.

2

Parathyroid hormone-dependent hypercalcemia.

Toke J, Patócs A, Balogh K, Gergics P, Stenczer B, Rácz K, Tóth M. Toke J, et al. Wien Klin Wochenschr. 2009;121(7-8):236-45. doi: 10.1007/s00508-009-1149-z. Wien Klin Wochenschr. 2009. PMID: 19562279 Review.

3

Rare diseases caused by abnormal calcium sensing and signalling.

Tőke J, Czirják G, Enyedi P, Tóth M. Tőke J, et al. Endocrine. 2021 Mar;71(3):611-617. doi: 10.1007/s12020-021-02620-5. Epub 2021 Feb 2. Endocrine. 2021. PMID: 33528764 Free PMC article. Review.

4

Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma.

Pálla S, Tőke J, Bozsik A, Butz H, Papp J, Likó I, Kuroli E, Bánvölgyi A, Hamar M, Bertherat J, Medvecz M, Patócs A. Pálla S, et al. Among authors: toke j. Sci Rep. 2023 Sep 5;13(1):14658. doi: 10.1038/s41598-023-41878-9. Sci Rep. 2023. PMID: 37670105 Free PMC article.

5

[Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia].

Doleschall M, Török D, Mészáros K, Luczay A, Halász Z, Németh K, Szücs N, Kiss R, Tőke J, Sólyom J, Fekete G, Patócs A, Igaz P, Tóth M. Doleschall M, et al. Among authors: toke j. Orv Hetil. 2018 Feb;159(7):269-277. doi: 10.1556/650.2018.30986. Orv Hetil. 2018. PMID: 29429350 Review. Hungarian.

6

[Significance of biochemical markers in the diagnosis of neuroendocrine tumours and for the follow-up of patients].

Tőke J, Czirják G, Tóth M, Rácz K, Patócs A. Tőke J, et al. Orv Hetil. 2014 Nov 9;155(45):1775-82. doi: 10.1556/OH.2014.30035. Orv Hetil. 2014. PMID: 25362640 Review. Hungarian.

7

[Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency].

Tőke J, Bertalan R, Gergics P, Halász Z. Tőke J, et al. Orv Hetil. 2018 Feb;159(7):278-284. doi: 10.1556/650.2018.31029. Orv Hetil. 2018. PMID: 29429351 Review. Hungarian.

8

Parathyroid cancer with MTOR gene mutation: Case report and review of the literature.

Stark J, Tőke J, Huszty G, Nagy P, Bedics G, Bödör C, Tímár J, Tóth M. Stark J, et al. Among authors: toke j. Ann Endocrinol (Paris). 2023 Dec;84(6):761-763. doi: 10.1016/j.ando.2023.06.003. Epub 2023 Jun 24. Ann Endocrinol (Paris). 2023. PMID: 37500361 Review. No abstract available.

9

[CYP24A1 gene defect manifesting with gestational hypercalcemia].

Györkös A, Tőke J, Sohár G, Kovács M, Goldfinger J, Vajda G, Kalmár T, Tóth M. Györkös A, et al. Among authors: toke j. Orv Hetil. 2022 Jul 31;163(31):1237-1242. doi: 10.1556/650.2022.32520. Print 2022 Jul 31. Orv Hetil. 2022. PMID: 35908214 Hungarian.

10

Multiple bronchial carcinoids associated with Cowden syndrome.

Tömböl Z, Tőke J, Tóth G, Varga Z, Balázs E, Tóth E, Gergely L, Danihel Ľ, Medvecz M, Borka K, Tóth M. Tömböl Z, et al. Among authors: toke j. Endocrine. 2024 Feb 14. doi: 10.1007/s12020-024-03693-8. Online ahead of print. Endocrine. 2024. PMID: 38353885

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