АВТОРСКИ СВИДЕТЕЛСТВА
- M. Иванова. Авторско свидетелство № 4070/ 08.06.1987: ”Метод за получаване на катализатор за Циклизация на 1,3-бутадиен”
- M. Иванова. Авторско свидетелство № 90891/ 12.03.1991: “Метод за получаване на циклододекан”.
СЪАВТОР В НАУЧНИ КНИГИ, УЧЕБНИЦИ И ПОМАГАЛА
- Редки генетични болести в две части. Под редакцията на Проф. Д. Тончева, Изд. Къща „Симпелпрес“, София (2014) ISBN 978-619-183-012-1
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Медицинска генетика в клиничната практика: Ръководство за лекари и студенти. Издателска къща CIELA София (1999)
ISBN 954-649-199-3 -
“Педиатрия: Учебник за студенти по медицина, Първо издание, „Арбилис“, Септември 2019
ISBN: 978-619-7063-32-5
ПУБЛИКАЦИИ В НАУЧНИ СПИСАНИЯ
- 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
- 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
- Т. Делчев, Д. Авджиева, А. Кадъм, М. Иванова, Д. Илиев, Р. Тинчева. Орнитинтранскарбамилазен дефицит. Клиничен случай; Практическа педиатрия, 9, 2018, ХХ, 24-26
- 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
- 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
- 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.
- 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).
- 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
- 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
- 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
- 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
- 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
- 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).
- 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
- I. Singerska, R. Vajarova, I. Bradinova, M. Ivanova, I. Hasanova, I. Kremenski: Laboratory approach to lysosomal storage diseases diagnostics. Pediatriya 01/2011; 51(1).
- M. Ivanova, I. Bradinova, R. Vajarova, D. Dimitrov, I. Sinigerska, I. Kremenski: Hyperammonemia - Urea cycle disorders, diagnostic aproach. Pediatriya 01/2011; 51(1).
- 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.
- 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.
- 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
- M. Ivanova, I. Kremensky: Gas chromatography-mass spectrometry for diagnosis of X-linked adrenoleukodystrophy in Bulgaria. Pediatriya 01/2008; 48(1).
- R. Tincheva, M. Ivanova, V. Konstantinova, R. Georgieva: Case with pyruvate dehydrogenase deficiency. Pediatriya 01/2005; 45(3).
- 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
- 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
- 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
- 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
- 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
- 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).
- 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
- 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
- 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
- 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
- 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
- M. Ivanova, P.Yanakiev, E. Michaylova, I. Kremensky, Diagnosis of Organic Acidurias in Bulgaria,Balkan Journal of Medical Genetics, 1 (3), 1998: 128-1
- I.Kremensky, P. Janakiev, D. Grancharova, M. Ivanova, MCAD G985 mutation in Bulgarian population. Balkan Journal of Medical Genetics, 1(1), 1998: 18-20
- E. Michaylova, M. Ivanova, I. Kremensky, Identification of Organic acidurias by GC-MS. Balkan Journal of Clinical Laboratory, 5(2), 1997: