Начало / Университетът / Факултети / Факултет по химия и фармация / Структура / Катедри / Аналитична химия / Преподаватели / доц. д-р Мария Иванова / Списък с публикации

   

АВТОРСКИ СВИДЕТЕЛСТВА

 

  1. M. Иванова. Авторско свидетелство № 4070/ 08.06.1987: ”Метод за получаване на катализатор за Циклизация на 1,3-бутадиен”
  2. M. Иванова. Авторско свидетелство № 90891/ 12.03.1991: “Метод за получаване на циклододекан”.

 

СЪАВТОР В НАУЧНИ КНИГИ, УЧЕБНИЦИ И ПОМАГАЛА
  1. Редки генетични болести в две части. Под редакцията на Проф. Д. Тончева, Изд. Къща „Симпелпрес“, София (2014) ISBN 978-619-183-012-1
  2. Медицинска генетика в клиничната практика: Ръководство за лекари и студенти. Издателска къща CIELA София (1999)
    ISBN 954-649-199-3
  3. “Педиатрия: Учебник за студенти по медицина, Първо издание, „Арбилис“, Септември 2019
    ISBN: 978-619-7063-32-5

 

ПУБЛИКАЦИИ В НАУЧНИ СПИСАНИЯ

  1. Ivanova, M., I. Sinigerska, D. Dimitrov, V. Jordanova, I. Kremensky: Inhereted Errors of Metabolim – Metabolomic Approuch for Diagnosis in Bulgaria, Pediatria, 4/ 2018, vol. LVIII , 6-10, ISSN0479-7876
  2. М. Иванова, Ив. Синигерска, Д. Димитров, В. Йорданова, И. Кремeнски Вроден грешки на обмяната. Метаболитна криза- метаболомен подход за диагностика в България; Практическа педиатрия, 9, 2018, ХХ, 10-13
  3. Т. Делчев, Д. Авджиева, А. Кадъм, М. Иванова, Д. Илиев, Р. Тинчева. Орнитинтранскарбамилазен дефицит. Клиничен случай; Практическа педиатрия, 9, 2018, ХХ, 24-26
  4. Angelina Mandadzhieva, Daniela Avdzhieva-Tzavella, Tihomir Todorov, Savina Tincheva, Vanya Sinigerska, Mariya Ivanova, Alexey Savov, Vanyo Mitev, Albena Todorova: Wolman Disease in Bulgarian Patients: Selective Genetic Screening in Two Presumable Endemic Regions(2017); American Journal of Molecular Biology, 2017, 7, 169-175 http://www.scirp.org/journal/ajmb
  5. Penchev, V., Boueva, A., Kamenarova, K., Roussinov, D., Tzveova, R., Ivanova, M., Dimitrova, V., Kremensky, I., Mitev, V., Kaneva, R., Beltcheva, O. A familial case of severe infantile nephronophthisis explained by oligogenic inheritance (2017) European Journal of Medical Genetics, 60 (6), pp. 321-325. DOI: 10.1016/j.ejmg.2017.04.002
  6. Pacheva, I., Ivanov, I., Penkov, M., Kancheva, D., Jordanova, A., Ivanova, M. Creatine deficiency syndrome could be missed easily: A case report of guanidinoacetate methyltransferase deficiency presented with neurodevelopmental delay, seizures, and behavioral changes, but normal structural MRI (2016) Annals of Clinical and Laboratory Science, 46 (5), pp. 557-561.
  7. Daniela Avdjieva-Tzavella, Albena Todorova, Hadil Kathom, Maria Ivanova, Iglika Yordanova, Tihomir Todorov, Ivan Litvinenko, Anna Dasheva-Dimitrova, Radka Tincheva: Barth syndrome in male and female siblings caused by a novel mutation in the TAZ gene. Genetic counseling (Geneva, Switzerland) (2016) 12/2016; 27(4).
  8. Zerjav Tansek, M., Groselj, U., Angelkova, N., Anton, D., Baric, I., Djordjevic, M., Grimci, L., Ivanova, M., Kadam, A.,at al. Phenylketonuria screening and management in southeastern Europe - Survey results from 11 countries; (2015) Orphanet Journal of Rare Diseases, 10 (1), art. no. 68, . DOI: 10.1186/s13023-015-0283-0 MZ
  9. Ivan S. Ivanov, Dimitar N. Azmanov, Mariya B. Ivanova, at al: Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children (2014). Molecular Genetics and Metabolism, 113(1-2 SI), 2014: 76-83, DOI:10.1016
  10. Urh Groselj, Mojca Zerjav Tansek, Andraz Smon, Natalija Angelkova, Dana Anton, Ivo Baric, Maja Djordjevic, Lindita Grimci, Maria Ivanova, at al.: Newborn screening in southeastern Europe. Molecular Genetics and Metabolism 09/2014; 113(1-2), 42-45, DOI:10.1016/j.ymgme.2014.07.020
  11. D.M. AVDJIEVA-TZAVELLA, M.B. IVANOVA, T.P. TODOROV, A.P. TODOROVA, E.I. PANTELEEVA, S.S. TINCHEVA, E.A. LAZAROVA, H.M. KATHOM, P.G. YANEVA 5 AND R.S. TINCHEVA: First Bulgarian case of citrin deficiency caused by one novel and one recurrent mutation in the SLC25A13 gene. Genetic counseling (Geneva, Switzerland) 11/2014; 25(3), 271-276
  12. Stamenova Sv, Bojinova V., Stancheva M., Georgiev D., Milanov I., Shokova A., Ivanova M., Sinigerska I., Simeonov E. [Megalencephalic leukoecephalopathy with subcortical cysts: New clinical case from Bulgaria] Мегаленцефална левкодистрофия със субкортикални кисти: нов клиничен случаи от България. Българска неврология. Bulgarian Neurology, 14/3, 2013: 154-157
  13. D. Tzoneva, V. Guergueltcheva, I. Litvinenko, M. Ivanova, S. Hinev: Sedation for magnetic resonance imaging study in paediatric patients with neurological disorders. Pediatriya 01/2012; 52(4).
  14. David M S McHugh, Cynthia A Cameron, Jose E Abdenur, Mahera Abdulrahman…., Maria Ivanova, et al: Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project. Genetics in medicine: official journal of the American College of Medical Genetics 02/2011; 13(3)., DOI:10.1097/GIM.0b013e31820d5e67
  15. I. Singerska, R. Vajarova, I. Bradinova, M. Ivanova, I. Hasanova, I. Kremenski: Laboratory approach to lysosomal storage diseases diagnostics. Pediatriya 01/2011; 51(1).
  16. M. Ivanova, I. Bradinova, R. Vajarova, D. Dimitrov, I. Sinigerska, I. Kremenski: Hyperammonemia - Urea cycle disorders, diagnostic aproach. Pediatriya 01/2011; 51(1).
  17. Kremenski, R. Vajarova, I. Brandinova, M. Ivanova, I. Sinigerska, D. Dimitrov, A. Savov, S. Bichev, S. Andonova: Current tools for screening and diagnosis of inborn errors of metabolism. Pediatriya 01/2010; 50.
  18. R. Vajarova, I. Brandinova, A. Savov, S. Bichev, I. Singerska, M. Ivanova, I. Kremenski: Current tools for genetic diagnosis in idiopathic mental retardation. Pediatriya 01/2010; 50.
  19. S. S. Atanassova, P. Panchev, M. Ivanova: Plasma levels and urinary excretion of amino acids by subjects with renal calculi. Amino Acids 09/2009; 38(5)., DOI:10.1007/s00726-009-0359
  20. M. Ivanova, I. Kremensky: Gas chromatography-mass spectrometry for diagnosis of X-linked adrenoleukodystrophy in Bulgaria. Pediatriya 01/2008; 48(1).
  21. R. Tincheva, M. Ivanova, V. Konstantinova, R. Georgieva: Case with pyruvate dehydrogenase deficiency. Pediatriya 01/2005; 45(3).
  22. M. Ivanova, I. Sinigerska, I. Hasanova, I. Kremensky, Selective Screening for Diagnostics of Inherited Metabolic Diseases in Bulgaria Advances in Bulgarian Science, 3-4, 2005: 56
  23. Kremensky, A.Todorova, A. Jordanova, A. Savov, I. Tarnev, S. Iankova, B. Georgieva, B. Zaharova, R. Kaneva, R. Petkova, S. Andonova, M.Ivanova, N. Ivanova, R. Rainova and L. Kalaydjieva, Spectrum of Mutations of the most Common Genetic Disorders in Bulgaria. Journal for Quality of Life Research, 1(2), 2003: 172-18
  24. L. Angelova, E.Michaylova, E. Stephanova, M.Ivanova, B. Molzer and I.Kremensky, X-linked Adrenoleokodystrophy: Unusual Clinical Manifestation. Journal of Endocrine Genetics, 4 (2), 2001:1-4 http://www.researchgate.net/journal/1565-012X_Journal_of_Endocrine_Genetics_The
  25. V Mazneikova, V Dimitrova, Zh Karag'ozova, M Ivanova, E Mikhailova, A Stefanova, B Sl'ncheva, K Tsekova, S Lekova, Ts Furnadzhieva: [Pregnancy with Rh-isoimmunization. Results of a retrospective analysis in the maternity hospital "Maichin Dom"]. Akusherstvo i ginekologiia 02/2001; 40(3), 3-7
  26. L. Angelova, E. Michaylova, E. Stephanova, M. Ivanova, B. Molzer, I. Kremensky: X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation. International Journal on Disability and Human Development 01/2001; 2(4)., DOI:10.1515/IJDHD.2001.2.4.247
  27. Kremensky I, Jordanova A, Michaylova E, Todorova A, Ivanova M, Petkova R, Andonova S, Savov A, Zaharova B, Iankova S, Kaneva R, Kalaydjieva L: Laboratory diagnosis of inherited disorders and congenital anomalies in Bulgaria. Balkan Journal of Medical Genetics 01/2000; 4 (Number Vol.3 (4), 2000).
  28. Kremensky I, Jordanova A, Todorova A, Savov A, Iankova S, Georgieva B, Zaharova B, Kaneva R, Petkova R, Andonova S, Ivanova M, Michaylova E, Ivanova N, Kalaydjieva L.: Mutation profile of the most common genetic disorders in Bulgaria. Balkan Journal of Medical Genetics 01/2000; 4 (Number Vol.3 (4),3-12
  29. E. Paskalev, M. Ivanova, I. Kremenski: Plasma amino acid levels in patients on periodic hemodialysis treatment; Nephrology, hemodialysis and transplantasion, 5,1999 (3), 23-26
  30. Dimitrova V, Ivanova M, Kremensky I., The impact of establishing local medians for biochemical markers on false positive rate in Down's syndrome serum screening. Balcan Journal of Medical Genetics, 1999
  31. B. Radeva, M. Natcheva, W. Lehnert, I. Kremensky, E. Michaylova, M. Ivanova: Canavan disease and erythrodermia ichthyosiformis. Clinical picture, diagnosis and treatment of Inherited metabolic diseases in infancy Part I, 1998; 113-116
  32. Kremensky I, Ivanova M, Michajlova E.The Bulgarian programme for selective metabolic screening of inborn errors of metabolism. Balkan Journal of Medical Genetics, Vol 5(2), 160, 1998
  33. M. Ivanova, P.Yanakiev, E. Michaylova, I. Kremensky, Diagnosis of Organic Acidurias in Bulgaria,Balkan Journal of Medical Genetics, 1 (3), 1998: 128-1
  34. I.Kremensky, P. Janakiev, D. Grancharova, M. Ivanova, MCAD G985 mutation in Bulgarian population. Balkan Journal of Medical Genetics, 1(1), 1998: 18-20
  35. E. Michaylova, M. Ivanova, I. Kremensky, Identification of Organic acidurias by GC-MS. Balkan Journal of Clinical Laboratory, 5(2), 1997:

 

 

Публикуван:

Савина Кирилова

05.03.2020 1:04 pm


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