المؤلفون: Olgac A, Okur İ, Biberoğlu G, Ezgü FS, Tümer L

المصدر: Balkan Journal of Medical Genetics, Vol 24, Iss 1, Pp 103-106 (2021)

مصطلحات موضوعية: familial chylomicronemia syndrome (fcs), glycogen storage disease type 1a (gsd1a), hypertriglyceridemia (htg), pancreatitis, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1311-0160

URL الوصول: https://doaj.org/article/520bfc7158984610bff713d9df79e5b1

المؤلفون: Olgac A, Tekin Orgun L, Ezgü FS, Biberoǧlu G, Tümer L

المصدر: Balkan Journal of Medical Genetics, Vol 22, Iss 2, Pp 93-96 (2019)

مصطلحات موضوعية: inborn errors of metabolism, l-2-hydroxyglutaric aciduria (l2hga), seizure, tremor, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1311-0160

URL الوصول: https://doaj.org/article/f27513f6cfb84b3da5b73d7d92b06d8f

المؤلفون: Kasapkara, Ç S, Cinasal Demir, G, Hasanoğlu, A, Tümer, L

المصدر: European Journal of Clinical Nutrition ; volume 68, issue 1, page 101-105 ; ISSN 0954-3007 1476-5640

الاتاحة: http://dx.doi.org/10.1038/ejcn.2013.186
https://www.nature.com/articles/ejcn2013186
https://www.nature.com/articles/ejcn2013186.pdf

المؤلفون: Tümer, L, Vuralli, D, Hasanoğlu, A, Biberoğlu, G, Ilhan, M

المصدر: Pediatric Research ; volume 68, page 195-195 ; ISSN 0031-3998 1530-0447

الاتاحة: http://dx.doi.org/10.1203/00006450-201011001-00378

المؤلفون: Küçükçongar A., Yenicesu I., Tümer L., Kasapkara C.S., Ezgü F.S., Paşaoglu O., Demirtaş C.

المساهمون: Küçükçongar A., Yenicesu I., Tümer L., Kasapkara C.S., Ezgü F.S., Paşaoglu O., Demirtaş C., Zonguldak Bülent Ecevit Üniversitesi

مصطلحات موضوعية: Adhesion molecules, Apheresis, Children, Homozygous hypercholesterolemia

Relation: Transfusion and Apheresis Science; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; 391; 396; 48; https://dx.doi.org/10.1016/j.transci.2013.04.024; https://hdl.handle.net/20.500.12628/4322

الاتاحة: https://hdl.handle.net/20.500.12628/4322
https://doi.org/10.1016/j.transci.2013.04.024

المؤلفون: Ezgü, F.S., Atalay, Y., Hasanoğlu, A., Gücüyener, K., Biberoğlu, G., Koç, E., Ergenekon, E., Tümer, L.

المصدر: Nutritional Neuroscience ; volume 7, issue 5-6, page 351-356 ; ISSN 1028-415X 1476-8305

الاتاحة: http://dx.doi.org/10.1080/10284150400017280
http://www.tandfonline.com/doi/pdf/10.1080/10284150400017280

المؤلفون: Küçükçongar, A, Tümer, L, Ezgü, F Süheyl, Kasapkara, Ç Seher, Jaeken, Jaak, Matthijs, Gert, Rymen, Daisy, Dalgiç, B, Bıdecı, A, Hasanoğlu, A

وصف الملف: 168347 bytes; application/pdf

Relation: Genetic Counseling vol:26 issue:1 pages:87-90; https://lirias.kuleuven.be/handle/123456789/499828; https://lirias.kuleuven.be/bitstream/123456789/499828/1//Kucukcongar+Genet+Couns+2015.pdf

الاتاحة: https://lirias.kuleuven.be/handle/123456789/499828
https://lirias.kuleuven.be/bitstream/123456789/499828/1//Kucukcongar+Genet+Couns+2015.pdf

المؤلفون: Kasapkara, C S, Tümer, L, Ezgü, F S, Hasanoğlu, A, Race, V, Matthijs, Gert, Jaeken, Jaak

Relation: European Journal of Paediatric Neurology vol:16 issue:5 pages:554-556; https://lirias.kuleuven.be/handle/123456789/335166; http://linkinghub.elsevier.com/retrieve/pii/S1090-3798(11)00258-3; https://lirias.kuleuven.be/bitstream/123456789/335166/3//Kasapkara+Eur+J+Paed+Neurol+2012.pdf

الاتاحة: https://lirias.kuleuven.be/handle/123456789/335166
http://linkinghub.elsevier.com/retrieve/pii/S1090-3798(11)00258-3
https://lirias.kuleuven.be/bitstream/123456789/335166/3//Kasapkara+Eur+J+Paed+Neurol+2012.pdf

المؤلفون: Kasapkara, C.S., Tümer, L., Ezgü, F.S., Hasanoğlu, A., Race, V., Matthijs, G., Jaeken, J.

المصدر: European Journal of Paediatric Neurology ; volume 16, issue 5, page 554-556 ; ISSN 1090-3798

الاتاحة: http://dx.doi.org/10.1016/j.ejpn.2011.12.011
https://api.elsevier.com/content/article/PII:S1090379811002583?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1090379811002583?httpAccept=text/plain

المؤلفون: Küçükçongar, A., Ezgü, F.S., Tümer, L., Dalgıç, B., Hasanoğlu, A.

المصدر: Clinical Therapeutics ; volume 34, issue 4, page e23-e24 ; ISSN 0149-2918

الاتاحة: http://dx.doi.org/10.1016/j.clinthera.2012.03.043
https://api.elsevier.com/content/article/PII:S0149291812001932?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0149291812001932?httpAccept=text/plain

المؤلفون: Cs Kasapkara, Tümer, L., Küçükçongar, A., Hasanoğlu, A., Sara Seneca, Linda De Meirleir

المساهمون: Department of Embryology and Genetics, Reproduction and Genetics, Pediatrics, Neurogenetics

المصدر: Vrije Universiteit Brussel

مصطلحات موضوعية: mitochiindrial DNA depletion, DGUOK, MDDS

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3493b29822cd35697b5d435dd4690808
https://biblio.vub.ac.be/vubir/dguok-related-mitochondrial-depletion-syndrome-in-a-child-with-an-early-diagnosis-of-gsd(a9ca3032-12d3-41e4-8f15-5bf111be39a4).html

المؤلفون: Ezgü, F., Tümer, L., Ozbay, F., Hasanoğlu, A., Biberoğlu, G., Aybay, C.

المصدر: Journal of Pediatric Endocrinology and Metabolism ; volume 22, issue 10 ; ISSN 2191-0251 0334-018X

الاتاحة: http://dx.doi.org/10.1515/jpem.2009.22.10.915
https://www.degruyter.com/document/doi/10.1515/JPEM.2009.22.10.915/pdf

المؤلفون: Aktürk, A., Arhan, E., Eminoğlu, T., Biberoğlu, G., Serdaroğlu, A., Tümer, L., Hasanoğlu, A., Demir, E., Gücüyener, K.

المصدر: European Journal of Paediatric Neurology ; volume 11, page 67 ; ISSN 1090-3798

الاتاحة: http://dx.doi.org/10.1016/s1090-3798(08)70501-4
https://api.elsevier.com/content/article/PII:S1090379808705014?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1090379808705014?httpAccept=text/plain

المؤلفون: Gunduz, M., Paschke, E., Fatih, Atuek, Tuemer, L., Hasanodlu, A., Ezgu, FATİH SÜHEYL

Relation: 97ac5159-1def-4730-befd-506d21bf5c54; https://avesis.gazi.edu.tr/publication/details/97ac5159-1def-4730-befd-506d21bf5c54/oai

الاتاحة: https://avesis.gazi.edu.tr/publication/details/97ac5159-1def-4730-befd-506d21bf5c54/oai

المؤلفون: Ezgü, Fs., Tümer, L., Hasanglu, A., Gündüz, M., Tyras, U., Ünsal, R., Seneca, Sara

المساهمون: Department of Embryology and Genetics

مصطلحات موضوعية: BCS1L gene mutation, mt disorders, sodium bicarbonate, complex III deficiency

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3848::de2176f98fee7d4cc852056366582c58
https://biblio.vub.ac.be/vubir/severe-renal-tubulopathy-and-cholestasis-due-to-bcs1l-gene-mutation-of-complex-iii-experience-with-high-dose-sodium-bicarbonate-therapy(0147d192-68c4-4a92-85ca-65e7e407bbe2).html

المؤلفون: Tümer, L, Serdaroğlu, A, Hasanoğlu, A, Biberoğlu, G, Aksoy, E

المصدر: Acta Paediatrica ; volume 91, issue 9, page 923-926 ; ISSN 0803-5253

الاتاحة: http://dx.doi.org/10.1080/080352502760272597
http://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1080%2F080352502760272597

المؤلفون: Bideci, A., Cinaz, P., Hasanoğlu, A., Tümer, L.

المصدر: Journal of Pediatric Endocrinology and Metabolism ; volume 15, issue 1 ; ISSN 2191-0251 0334-018X

الاتاحة: http://dx.doi.org/10.1515/jpem.2002.15.1.41
https://www.degruyter.com/document/doi/10.1515/JPEM.2002.15.1.41/pdf

المؤلفون: Hasanoǧlu, A., Bideci, A., Cinaz, P., Tümer, L., Ünal, S.

المصدر: Journal of Pediatric Endocrinology and Metabolism ; volume 13, issue 3 ; ISSN 2191-0251 0334-018X

الاتاحة: http://dx.doi.org/10.1515/jpem.2000.13.3.307
https://www.degruyter.com/document/doi/10.1515/JPEM.2000.13.3.307/pdf

المؤلفون: Erbayat Altay, E., Serdaroğlu, A., Tümer, L., Gücüyener, Κ., Hasanoğlu, A.

المصدر: Journal of Pediatric Endocrinology and Metabolism ; volume 13, issue 7 ; ISSN 2191-0251 0334-018X

الاتاحة: http://dx.doi.org/10.1515/jpem.2000.13.7.933
https://www.degruyter.com/document/doi/10.1515/JPEM.2000.13.7.933/pdf

المؤلفون: Tümer, L., Hasanoğlu, A., Cinaz, P., Bideci, A.

المصدر: Journal of Pediatric Endocrinology and Metabolism ; volume 12, issue 4 ; ISSN 2191-0251 0334-018X

الاتاحة: http://dx.doi.org/10.1515/jpem.1999.12.4.519
https://www.degruyter.com/document/doi/10.1515/JPEM.1999.12.4.519/pdf