Počet záznamov: 1
Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriers.
Názov Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriers. Autor Staník Juraj SAVEXEND - Ústav experimentálnej endokrinológie SAV Spoluautori Gašperíková Daniela SAVEXEND - Ústav experimentálnej endokrinológie SAV RID ORCID Pašková M. Barák L. Javorková J. Jancová E. Flanagan S.E. Hattersley A. T. Ellard S. Klimeš Iwar SAVEXEND - Ústav experimentálnej endokrinológie SAV Spoluautori Ciljaková M. Hlava P. Michálek J. Pearson E. Zdroj.dok. Journal of Clinical Endocrinology & Metabolism. Vol. 92, no. 4 (2007), p. 1276-1282 Jazyk dok. eng - angličtina Krajina US - Spojené štáty Druh dok. rozpis článkov z periodík (rbx) Ohlasy MALECKI, M. T. The search for undiagnosed MODY patients: what is the next step?. In DIABETOLOGIA, 2010, vol.53, no.12, 2465-2467. QUAN, Yi - BARSZCZYK, Andrew - FENG, Zhong-ping - SUN, Hong-shuo. Current understanding of K-ATP channels in neonatal diseases: focus on insulin secretion disorders. In ACTA PHARMACOLOGICA SINICA, 2011, vol.32, no.6, 765-780. RUBIO-CABEZAS, Oscar - KLUPA, Tomasz - MALECKI, Maciej T. Permanent neonatal diabetes mellitus the importance of diabetes differential diagnosis in neonates and infants. In EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2011, vol.41, no.3, 323-333. LI, Cheng-Jiang - ZHOU, Hua-Li - LI, Jun - YAO, Hong-Tian - SU, Rong - LI, Wen-Peng. Roles of sulfonylurea receptor 1 and multidrug resistance protein 1 in modulating insulin secretion in human insulinoma. In HEPATOBILIARY & PANCREATIC DISEASES INTERNATIONAL, 2011, vol.10, no.1, 88-94. RUSSO, L. - IAFUSCO, D. - BRESCIANINI, S. - NOCERINO, V. - BIZZARRI, C. - TONI, S. - CERUTTI, F. - MONCIOTTI, C. - PESAVENTO, R. - IUGHETTI, L. - BERNARDINI, L. - BONFANTI, R. - GARGANTINI, L. - VANELLI, M. - AGUILAR-BRYAN, L. - STAZI, M. A. - GRASSO, V. - COLOMBO, C. - BARBETTI, F. Permanent diabetes during the first year of life: multiple gene screening in 54 patients. In DIABETOLOGIA, 2011, vol.54, no.7, 1693-1701. NAYLOR, Rochelle N. - GREELEY, Siri Atma W. - BELL, Graeme I. - PHILIPSON, Louis H. Genetics and pathophysiology of neonatal diabetes mellitus. In JOURNAL OF DIABETES INVESTIGATION, 2011, vol.2, no.3, 158-169. WATANABE, Richard M. Drugs, diabetes and pharmacogenomics: the road to personalized therapy. In PHARMACOGENOMICS, 2011, vol.12, no.5, 699-701. GREELEY S.A.W, TUCKER S.E, NAYLOR R.N, BELL G.I, PHILIPSON L.H: Neonatal diabetes mellitus: A model for personalized medicine. TRENDS IN ENDOCRINOLOGY AND METABOLISM 21 (8), pp. 464-472, 2010 LANG, V. - LIGHT, P.E. The molecular mechanisms and pharmacotherapy of ATP-sensitive potassium channel gene mutations underlying neonatal diabetes. In Pharmacogenomics and Personalized Medicine, 2010, vol.3, no.1, 145-161. VENDRAMINI, Marcio F. - GURGEL, Lucimary C. - MOISES, Regina S. Long-term response to sulfonylurea in a patient with diabetes due to mutation in the KCNJ11 gene. In ARQUIVOS BRASILEIROS DE ENDOCRINOLOGIA E METABOLOGIA, 2010, vol.54, no.8, 682-684. GREELEY, Siri Atma W. - TUCKER, Susan E. - WORRELL, Helen I. - SKOWRON, Kinga B. - BELL, Graeme I. - PHILIPSON, Louis H. Update in neonatal diabetes. In CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY, 2010, vol.17, no.1, 13-19. KLUPA, T. - SKUPIEN, J. - MIRKIEWICZ-SIERADZKA, B. - GACH, A. - NOCZYNSKA, A. - ZUBKIEWICZ-KUCHARSKA, A. - SZALECKI, M. - KOZEK, E. - NAZIM, J. - MLYNARSKI, W. - MALECKI, M.T. Efficacy and Safety of Sulfonylurea Use in Permanent Neonatal Diabetes Due to KCNJ11 Gene Mutations: 34-Month Median Follow-Up. In DIABETES TECHNOLOGY & THERAPEUTICS. ISSN 1520-9156, MAY 2010, vol. 12, no. 5, p. 387-391. AL-MAHDI, M. - AL MUTAIR, A. - AL BALWI, M. - HUSSAIN, K. Successful transfer from insulin to oral sulfonylurea in a 3-year-old girl with a mutation in the KCNJ11 gene. In ANNALS OF SAUDI MEDICINE. ISSN 0256-4947, MAR-APR 2010, vol. 30, no. 2, p. 162-164. LOOMBA-ALBRECHT, L.A. - GLASER, N.S. - STYNE, D.M. - BREMER, A.A. An Oral Sulfonylurea in the Treatment of Transient Neonatal Diabetes Mellitus. In CLINICAL THERAPEUTICS. ISSN 0149-2918, APR 2009, vol. 31, no. 4, p. 816-820. STOY, J. - GREELEY, S.A.W. - PAZ, V.P. - YE, H. - PASTORE, A.N. - SKOWRON, K.B. - LIPTON, R.B. - COGEN, F.R. - BELL, G.I. - PHILIPSON, L.H. Diagnosis and treatment of neonatal diabetes: an United States experience. In PEDIATRIC DIABETES. ISSN 1399-543X, OCT 2008, vol. 9, no. 5, p. 450-459. BREMER, A.A. - RANADIVE, S. - LUSTIG, R.H. Outpatient transition of an infant with permanent neonatal diabetes due to a KCNJ11 activating mutation from subcutaneous insulin to oral glyburide. In PEDIATRIC DIABETES. ISSN 1399-543X, JUN 2008, vol. 9, no. 3, Part 1, p. 236-239. RUBIO-CABEZAS, O. - GONZALEZ, F.D. - ARAGONES, A. - ARGENTE, J. - CAMPOS-BARROS, A. Permanent neonatal diabetes caused by a homozygous nonsense mutation in the glucokinase gene. In PEDIATRIC DIABETES. ISSN 1399-543X, JUN 2008, vol. 9, no. 3, Part 1, p. 245-249. AGUILAR-BRYAN, L. - BRYAN, J. Neonatal diabetes mellitus. In ENDOCRINE REVIEWS. ISSN 0163-769X, MAY 2008, vol. 29, no. 3, p. 265-291. JAFAR-MOHAMMADI, B. - MCCARTHY, M.I. Genetics of type 2 diabetes mellitus and obesity - a review. In ANNALS OF MEDICINE. ISSN 0785-3890, 2008, vol. 40, no. 1, p. 2-10. FLECHTNER, I. - VAXILLAIRE, M. - CAVE, H. - SCHARFMANN, R. - FROGUEL, P. - POLAK, M. Neonatal hyperglycaemia and abnormal development of the pancreas. In BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM. ISSN 1521-690X, FEB 2008, vol. 22, no. 1, p. 17-40. FLECHTNER, I. - VAXILLAIRE, M. - CAVE, H. - SCHARFMANN, R. - FROGUEL, P. - POLAK, M. Diabetes in very young children and mutations in the insulin-secreting cell potassium channel genes: Therapeutic consequences. In DEVELOPMENT OF THE PANCREAS AND NEONATAL DIABETES. ISSN 1421-7082, 2007, vol. 12, p. 86-98. POLAK, M. Neonatal diabetes mellitus: Insights for more common forms of diabetes. In JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. ISSN 0021-972X, OCT 2007, vol. 92, no. 10, p. 3774-3776. SUZUKI, S. - MAKITA, Y. - MUKAI, T. - MATSUO, K. - UEDA, O. - FUJIEDA, K. Molecular basis of neonatal diabetes in Japanese patients. In JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. ISSN 0021-972X, OCT 2007, vol. 92, no. 10, p. 3979-3985. DE BUNT, M.V. - GLOYN, A.L. Monorenic disorders of the pancreatic beta-cell: personalizing treatment for rare forms of diabetes and hypoglycemia. In PERSONALIZED MEDICINE. ISSN 1741-0541, AUG 2007, vol. 4, no. 3, p. 247-259. MAK, CM; LEE, CY; LAM, CW; SIU, WK; HUNG, VCN; CHAN, AYW.: Personalized Medicine Switching from Insulin to Sulfonylurea in Permanent Neonatal Diabetes Mellitus Dictated by a Novel Activating ABCC8 Mutation. DIAGNOSTIC MOLECULAR PATHOLOGY 21 (1), pp. 56-59 JAVORSKY, M; KLIMCAKOVA, L; SCHRONER, Z; ZIDZIK, J; BABJAKOVA, E; FABIANOVA, M; KOZAROVA, M; TKACOVA, R; SALAGOVIC, J; TKAC, I.: KCNJ11 gene E23K variant and therapeutic response to sulfonylureas. EUROPEAN JOURNAL OF INTERNAL MEDICINE 23 (3), pp. 245-249 OOI, HOOI LENG; WU, LOO LING.: Three cases of permanent neonatal diabetes mellitus: genotypes and management outcome. SINGAPORE MEDICAL JOURNAL 53 (7), pp. E142-E144 IAFUSCO, D; MASSA, O; PASQUINO, B; COLOMBO, C; IUGHETTI, L; BIZZARRI, C; MAMMI, C; LO PRESTI, D; SUPRANI, T; SCHIAFFINI, R; NICHOLS, CG; RUSSO, L; GRASSO, V; MESCHI, F; BONFANTI, R; BRESCIANINI, S; BARBETTI, F.: Minimal incidence of neonatal/infancy onset diabetes in Italy is 1:90,000 live births. ACTA DIABETOLOGICA 49 (5), pp. 405-408 ABDEL-SALAM, GMH; SCHAFFER, AE; ZAKI, MS; DIXON-SALAZAR, T; MOSTAFA, IS; AFIFI, HH; GLEESON, JG.: A homozygous IER3IP1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS). AMERICAN JOURNAL OF MEDICAL GENETICS PART A 158A (11), pp. 2788-2796 MYSLIWIEC, M.: Modulators of K+ channels in diabetology. POTASSIUM CHANNELS AS A TARGET FOR CLINICAL THERAPEUTICS pp. 43-60 IRGENS, H. U. - MOLNES, J. - JOHANSSON, B. B. - RINGDAL, M. - SKRIVARHAUG, T. - UNDLIEN, D. E. - SOVIK, O. - JONER, G. - MOLVEN, A. - NJOLSTAD, P. R. Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry. In DIABETOLOGIA. ISSN 0012-186X, 2013, vol. 56, no. 7, pp. 1512. DI BENEDETTO, M. - RICHARD, O. - PELISSIER, P. - DARTEYRE, S. - CAVE, H. - STEPHAN, J-L. Permanent neonatal diabetes and recessive mutation in the INS gene: A familial history. In ARCHIVES DE PEDIATRIE. ISSN 0929-693X, 2013, vol. 20, no. 2, pp. 199. JAHNAVI, S. - POOVAZHAGI, V. - MOHAN, V. - BODHINI, D. - RAGHUPATHY, P. - AMUTHA, A. - KUMAR, P. Suresh - ADHIKARI, P. - SHRIRAAM, M. - KAUR, T. - DAS, A. K. - MOLNES, J. - NJOLSTAD, P. R. - UNNIKRISHNAN, R. - RADHA, V. Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children. In CLINICAL GENETICS. ISSN 0009-9163, 2013, vol. 83, no. 5, pp. 439. HABEB, Abdelhadi M. Frequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: A systematic review. In Libyan Journal of Medicine. ISSN 19932820, 2013, vol. 8, no. 1. PROKS, Peter. Neonatal diabetes caused by activating mutations in the sulphonylurea receptor. In Diabetes and Metabolism Journal. ISSN 22336079, 2013, vol. 37, no. 3, pp. 157-164. CAPPONI, Magdalena - QUIRÓS, Carmen - CONGET, Ignacio - ESMATJES, Enric - GIMÉNEZ, Marga. Reclassification and transfer from insulin to sulfonilureas in a KCNJ11 mutation after 15 years of insulin therapy | Reclasificación y transferencia de insulina a sulfonilureas en un paciente con mutación en KCNJ11 tras 15 años de tratamiento con insulina. In Avances en Diabetologia. ISSN 11343230, 2014, vol. 30, no. 4, pp. 115-117. SERRA-SOLER, Guillermo - MANGA, Bárbara - NAVARRO-FALCÓN, Magnolia - CODINA-MARCET, Mercè. Reclassification of a consistent neonatal type 1 diabetes mellitus and effective transfer from insulin to sulphonylurea | Reclasificación de una diabetes mellitus tipo 1 en diabetes neonatal permanente y transferencia efectiva de insulina a sulfonilurea. In Avances en Diabetologia. ISSN 11343230, 2014, vol. 30, no. 1, pp. 23-26. ESQUIAVETO-AUN, Adriana Mangue - DE MELLO, Maricilda Palandi - VANTI MACEDO PAULINO, Maria Fernanda - MINICUCCI, Walter Jose - GUERRA-JUNIOR, Gil - VALENTE DE LEMOS-MARINI, Sofia Helena. A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins. In DIABETOLOGY & METABOLIC SYNDROME. ISSN 1758-5996, 2015, vol. 7. MUSA, Noha - HAFEZ, Mona - HASSAN, Mona - EL-MOUGY, Fatma - SHARAF, Sahar - POLAK, Michael - CAVE, Helene - MOFEED, Sherif. Clinical, molecular, and therapeutic aspects of NDM in ten cases with diabetes in 1st 6 months of life. In INTERNATIONAL JOURNAL OF DIABETES IN DEVELOPING COUNTRIES. ISSN 0973-3930, 2016, vol. 36, no. 1, pp. 81-88. HUOPIO, Hanna - MIETTINEN, Paivi J. - ILONEN, Jorma - NYKANEN, Paivi - VEIJOLA, Riitta - KESKINEN, Paivi - NANTO-SALONEN, Kirsti - VANGIPURAPU, Jagadish - RAIVO, Joose - STANCAKOVA, Alena - MANNISTO, Jonna - KUULASMAA, Teemu - KNIP, Mikael - OTONKOSKI, Timo - LAAKSO, Markku. Clinical, Genetic, and Biochemical Characteristics of Early-Onset Diabetes in the Finnish Population. In JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. ISSN 0021-972X, 2016, vol. 101, no. 8, pp. 3018-3026. AL-AGHA, Abdulmoein E. - AHMAD, Ihab A. Clinical and genetic features of permanent neonatal diabetes mellitus. In INTERNATIONAL JOURNAL OF DIABETES IN DEVELOPING COUNTRIES. ISSN 0973-3930, 2016, vol. 36, no. 1, pp. 18-22. CHAI-UDOM, Rapeepun - SAHAKITRUNGRUANG, Taninee - WACHARASINDHU, Suttipong - SUPORNSILCHAI, Vichit. A girl with permanent neonatal diabetes due to KCNJ11 mutation presented with Mauriac syndrome after improper adjustment in sulfonylurea dosage over 6 years. In JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM. ISSN 0334-018X, 2016, vol. 29, no. 9, pp. 1095-1101. CARMODY, D. - PASTORE, A. N. - LANDMEIER, K. A. - LETOURNEAU, L. R. - MARTIN, R. - HWANG, J. L. - NAYLOR, R. N. - HUNTER, S. J. - MSALL, M. E. - PHILIPSON, L. H. - SCOTT, M. N. - GREELEY, S. A. W. Patients with KCNJ11-related diabetes frequently have neuropsychological impairments compared with sibling controls. In DIABETIC MEDICINE. ISSN 0742-3071, 2016, vol. 33, no. 10, pp. 1380-1386. ŠUMNÍK, Zdeněk - PRŮHOVÁ, Štěpánka - CINEK, Ondřej. Heterogeneity of childhood diabetes and its therapeutic implications. In Vnitrni Lekarstvi. ISSN 0042773X, 2016, vol. 66, no. 11, pp. 4S129-4S135. ZHANG, Hongliang - ZHONG, Xiaobin - HUANG, Zhenguang - HUANG, Chun - LIU, Taotao - QIU, Yue. Sulfonylurea for the treatment of neonatal diabetes owing to K-ATP-channel mutations: a systematic review and meta-analysis. In ONCOTARGET. ISSN 1949-2553, 2017, vol. 8, no. 64, pp. 108274-108285. BARBETTI, Fabrizio - MAMMI, Corrado - LIU, Ming - GRASSO, Valeria - ARVAN, Peter - REMEDI, Maria - NICHOLS, Colin G. Neonatal Diabetes: Permanent Neonatal Diabetes and Transient Neonatal Diabetes. In DIABETES ASSOCIATED WITH SINGLE GENE DEFECTS AND CHROMOSOMAL ABNORMALITIES. ISSN 0251-5342, 2017, vol. 25, pp. 1-25. MUKHERJEE, Soham - RASTOGI, Ashu - VENKATESAN, Radha - SUNDARAMOORTHI, Gopi - MOHAN, Viswanathan - BHANSALI, Anil. An infant with diabetes mellitus: Is it always T1DM? In DIABETES RESEARCH AND CLINICAL PRACTICE. ISSN 0168-8227, 2017, vol. 125, pp. 62-64. GUBAEVA, Diliara N. - LAPTEV, Dmitry N. - TIULPAKOV, Anatoly N. - PETROVA, Lidia M. SEVERE WOLCOTT-RALLISON SYNDROME DUE TO A NONSENSE MUTATION IN THE FIRST EXON EIF2AK3. In DIABETES MELLITUS. ISSN 2072-0351, 2018, vol. 21, no. 1, pp. 42-47. IOACARA, Sorin - SAVA, Elisabeta - BAROSAN, Alexandra - COJOCARU, Florentina - GUTAN, Adelina - FICA, Simona. To diet or not to diet in neonatal diabetes responding to sulfonylurea treatment. In Journal of Pediatric Endocrinology and Metabolism. ISSN 0334018X, 2018-09-01, 31, 9, pp. 1053-1056. NEU, Andreas - BUERGER-BUESING, Jutta - DANNE, Thomas - DOST, Axel - HOLDERS, Martin - HOLL, Reinhard W. - HOLTERHUS, Paul-Martin - KAPELLEN, Thomas - KARGES, Beate - KORDONOURI, Olga - LANGE, Karin - MUELLER, Susanne - RAILE, Klemens - SCHWEIZER, Roland - VON SENGBUSCH, Simone - STACHOW, Rainer - WAGNER, Verena - WIEGAND, Susanna - ZIEGLER, Ralph. Diagnosis, Therapy and Follow-up of Diabetes Mellitus in Children and Adolescents. In EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES. ISSN 0947-7349, 2019, vol. 127, no. 6, pp. 341-+. ISLEYEN, Fatih - BOLU, Semih. The Epidemiological Characteristics of Diabetic Children in the Province of Adiyaman. In GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS. ISSN 1304-9054, 2019, vol. 17, no. 1, pp. 1-16. AL-KHAWAGA, Sara - MOHAMMED, Idris - SARASWATHI, Saras - HARIS, Basma - HASNAH, Reem - SAEED, Amira - ALMABRAZI, Akeem - SYED, Najeeb - JITHESH, Puthen - EL AWWA, Ahmed - KHALIFA, Amal - ALKHALAF, Awziya - PETROVSKI, Goran - ABDELALIM, Ssam M. - HUSSAIN, Hatid. The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar. In MOLECULAR GENETICS & GENOMIC MEDICINE. ISSN 2324-9269, 2019, vol. 7, no. 10, pp. TORBJORNSDOTTER, Torun - MAROSVARI-BARNA, Elisabeth - HENCKEL, Ewa - CORRIAS, Martino - NORGREN, Svante - JANSON, Annika. Successful treatment of a cohort of infants with neonatal diabetes using insulin pumps including data on genetics and estimated incidence. In ACTA PAEDIATRICA. ISSN 0803-5253, 2020, vol. 109, no. 6, pp. 1131-1137. NEU, Andreas - BUERGER-BUESING, Jutta - DANNE, Thomas - DOST, Axel - HOLDER, Martin - HOLL, Reinhard W. - HOLTERHUS, Paul-Martin - KAPELLEN, Thomas - KARGES, Beate - KORDONOURI, Olga - LANGE, Karin - MUELLER, Susanne - RAILE, Klemens - SCHWEIZER, Roland - VON SENGBUSCH, Simone - STACHOW, Rainer - WAGNER, Verena - WIEGAND, Susanna - ZIEGLER, Ralph. Diagnosis, Therapy and Follow-Up of Diabetes Mellitus in Children and Adolescents. In EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES. ISSN 0947-7349, 2019, vol. 127, no., pp. S39-S72. HELMI, Muhd Alwi Muhd - HUSSAIN, Suhaimi. Severe Developmental Delay, Epilepsy and Neonatal Diabetes (DEND) Syndrome: A Case Report. In JOURNAL OF THE ASEAN FEDERATION OF ENDOCRINE SOCIETIES. ISSN 0857-1074, 2020, vol. 35, no. 1, pp. 125-128. BOLU, Semih - BUCAK, Ibrahim Hakan - KONCA, Capan - ELDEM, Irem - TEKIN, Mehmet. A novel de novo mutation at the ABCC8 gene in a newborn with transient diabetes mellitus. In TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS. ISSN 1306-0015, 2020, vol. 55, no. 2, pp. 195-198. MOULER, M. - LEBENTHAL, Y. - DE VRIES, L. - YACKOBOVITCH-GAVAN, M. - AVERBUCH, N.S. - FAURET-AMSELLEM, A.L. - CAVE, H. - BELTRAND, J. - POLAK, M. - PHILLIP, M. - NIMRI, R. Clinical characteristics, growth patterns, and long-term diabetes complications of 24 patients with neonatal diabetes mellitus: A single center experience. In PEDIATRIC DIABETES. ISSN 1399-543X, FEB 2022, vol. 23, no. 1, p. 45-54. Dostupné na: https://doi.org/10.1111/pedi.13295. RJIBA, K. - SOYAH, N. - KAMMOUN, M. - HMIDA, I.H. - SAAD, A. - MCELREAVEY, K. - MOUGOU-ZERELLI, S. Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian case. In EUROPEAN JOURNAL OF MEDICAL GENETICS. ISSN 1769-7212, SEP 2021, vol. 64, no. 9. Dostupné na: https://doi.org/10.1016/j.ejmg.2021.104285. NEU, A. - BURGER-BUSING, J. - DANNE, T. - DOST, A. - HOLDER, M. - HOLL, R.W. - HOLTERHUS, P.M. - KAPELLEN, T. - KARGES, B. - KORDONOURI, O. - LANGE, K. - MULLER, S. - RAILE, K. - SCHWEIZER, R. - VON SENGBUSCH, S. - STACHOW, R. - WAGNER, V. - WIEGAND, S. - ZIEGLER, R. Diagnosis, therapy and follow-up of diabetes mellitus in children and adolescents. In DIABETOLOGE. ISSN 1860-9716, JUL 2021, vol. 17, no. 5, SI, p. 557-584. Dostupné na: https://doi.org/10.1007/s11428-021-00769-1. REDDY, S. - MADDHURI, S. - NALLARI, P. - ANANTHAPUR, V. - KALYANI, S. - KRISHNA, M. - CHERKURI, N. - PATIBANDALA, S. Association of ABCC8 and KCNJ11 gene variants with type 1 diabetes in south Indians. In EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS. ISSN 1110-8630, APR 12 2021, vol. 22, no. 1. Dostupné na: https://doi.org/10.1186/s43042-021-00149-w. HOLDER, M. - KAPELLEN, T. - ZIEGLER, R. - BüRGER-BüSING, J. - DANNE, T. - DOST, A. - HOLL, R.W. - HOLTERHUS, P.M. - KARGES, B. - KORDONOURI, O. - LANGE, K. - MüLLER, S. - RAILE, K. - SCHWEIZER, R. - VON SENGBUSCH, S. - STACHOW, R. - WAGNER, V. - WIEGAND, S. - NEU, A. Diagnosis, Therapy and Follow-Up of Diabetes Mellitus in Children and Adolescents. In EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES. ISSN 0947-7349, SEP 2022, vol. 130, p. S49-S79. Dostupné na: https://doi.org/10.1055/a-1624-3388. NEU, A. - BüRGER-BüSING, J. - DANNE, T. - DOST, A. - HOLDER, M. - HOLL, R.W. - HOLTERHUS, P.M. - KAPELLEN, T. - KARGES, B. - KORDONOURI, O. - LANGE, K. - MüLLER, S. - RAILE, K. - SCHWEIZER, R. - VON SENGBUSCH, S. - STACHOW, R. - WAGNER, V. - WIEGAND, S. - ZIEGLER, R. Diagnosis, therapy and follow-up of diabetes mellitus in children and adolescents. In DIABETOLOGIE. ISSN 2731-7447, JUL 2022, vol. 18, no. 5, SI, p. 576-603. Dostupné na: https://doi.org/10.1007/s11428-022-00936-y. MARUCCI, A. - RUTIGLIANO, I. - FINI, G. - PEZZILLI, S. - MENZAGHI, C. - DI PAOLA, R. - TRISCHITTA, V. Role of Actionable Genes in Pursuing a True Approach of Precision Medicine in Monogenic Diabetes. In GENES. JAN 2022, vol. 13, no. 1. Dostupné na: https://doi.org/10.3390/genes13010117. Kategória ADCA - Vedecké práce v zahraničných karentovaných časopisoch impaktovaných Kategória (od 2022) V3 - Vedecký výstup publikačnej činnosti z časopisu Typ výstupu článok Rok vykazovania 2007 Registrované v WOS Registrované v SCOPUS Registrované v CCC DOI 10.1210/jc.2006-2490 
článok
rok CC IF IF Q (best) JCR Av Jour IF Perc SJR SJR Q (best) CiteScore A rok vydania rok metriky IF IF Q (best) SJR SJR Q (best) 2007 2006 5.799
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