Print preview VALIDITY EXPIRED personal data approved: 2021. XII. 09. Publications |
2021
from data base, 2021. XII. 09. |
Herold Zoltan, Doleschall Marton, Somogyi Aniko: Role and function of granin proteins in diabetes mellitus, WORLD JOURNAL OF DIABETES 12: (7) pp. 1081-1092. type of document: Journal paper/Review paper language: English URL |
2020
from data base, 2021. XII. 09. |
Herold Zoltan, Herold Magdolna, Rosta Klara, Doleschall Marton, Somogyi Aniko: Lower serum chromogranin B level is associated with type 1 diabetes and with type 2 diabetes patients with intensive conservative insulin treatment, DIABETOLOGY AND METABOLIC SYNDROME 12: (1) 61 type of document: number of independent citations: 3 language: English URL |
2020
from data base, 2021. XII. 09. |
Herold Zoltan, Herold Magdolna, Nagy Peter, Patocs Attila, Doleschall Marton, Somogyi Aniko: Serum chromogranin A level continuously rises with the progression of type 1 diabetes, and indicates the presence of both enterochromaffin‐like cell hyperplasia and autoimmune gastritis, JOURNAL OF DIABETES INVESTIGATION 11: (4) pp. 865-873. type of document: Journal paper/Article number of independent citations: 5 language: English URL |
2018
from data base, 2021. XII. 09. |
Doleschall Márton, Török Dóra, Mészáros Katalin, Luczay Andrea, Halász Zita, Németh Krisztina, Szücs Nikolette, Kiss Róbert, Tőke Judit, Sólyom János, Fekete György, Patócs Attila, Igaz Péter, Tóth Miklós: Szteroid-21-hidroxiláz-deficientia, a congenitalis adrenalis hyperplasia leggyakoribb oka [Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia], ORVOSI HETILAP 159: (7) pp. 269-277. type of document: Journal paper/Review paper number of independent citations: 3 language: Hungarian URL |
2017
from data base, 2021. XII. 09. |
Doleschall M, Luczay A, Koncz K, Hadzsiev K, Erhardt E, Szilagyi A, Doleschall Z, Nemeth K, Torok D, Prohaszka Z, Gereben B, Fekete G, Glaz E, Igaz P, Korbonits M, Toth M, Racz K, Patocs A: A unique haplotype of RCCX copy number variation, EUROPEAN JOURNAL OF HUMAN GENETICS 25: (6) pp. 702-710. type of document: Journal paper/Article number of independent citations: 3 language: English URL |
2014
from data base, 2021. XII. 09. |
Doleschall M, Szabo JA, Pazmandi J, Szilagyi A, Koncz K, Farkas H, Toth M, Igaz P, Glaz E, Prohaszka Z, Korbonits M, Racz K, Fust G, Patocs A: Common Genetic Variants of the Human Steroid 21-Hydroxylase Gene (CYP21A2) Are Related to Differences in Circulating Hormone Levels., PLOS ONE 9: (9) e107244 type of document: Journal paper/Article number of independent citations: 7 language: English URL |
2013
from data base, 2021. XII. 09. |
Banlaki Z, Szabo JA, Szilagyi A, Patocs A, Prohaszka Z, Fust G, Doleschall M: Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene, GENOME BIOLOGY AND EVOLUTION 5: (1) pp. 98-112. type of document: Journal paper/Article number of independent citations: 6 language: English URL |
2013
from data base, 2021. XII. 09. |
Szabo JA, Szilagyi A, Doleschall Z, Patocs A, Farkas H, Prohaszka Z, Racz K, Fust G, Doleschall M: Both Positive and Negative Selection Pressures Contribute to the Polymorphism Pattern of the Duplicated Human CYP21A2 Gene., PLOS ONE 8: (11) e81977 type of document: Journal paper/Article number of independent citations: 6 language: English URL |
2006
from data base, 2021. XII. 09. |
Zeöld A, Doleschall M, Haffner C, Capelo L, Menyhért J, Liposits Z, da Silva WS, Bianco AC, Kacskovics I, Fekete C, Gereben B: Characterization of the Nuclear Factor-κB Responsiveness of the Human dio2 Gene, ENDOCRINOLOGY 147: (9) pp. 4419-4429. type of document: Journal paper/Article number of independent citations: 36 language: English URL |
2004
from data base, 2021. XII. 09. |
Fekete C, Gereben B, Doleschall M, Harney JW, Dora JM, Bianco AC, Sarkar S, Liposits Z, Rand W, Emerson C, Kacskovics I, Larsen PR, Lechan RM: Lipopolysaccharide induces type 2 iodothyronine deiodinase in the mediobasal hypothalamus: Implications for the nonthyroidal illness syndrome, ENDOCRINOLOGY 145: (4) pp. 1649-1655. type of document: Journal paper/Article number of independent citations: 108 language: English URL |
| Number of independent citations to these publications: | 177 |
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