| An early manifestation of LBSL (leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation) syndrom, case description E Grechanina, E Zdubskaya | 1 | 2014 |
| Effectiveness of qualifying diagnostics of hereditary metabolic diseases with the use of gas chromatography/mass spectrometry by the example of the HHH syndrome E Grechanina, J Grechanina, O Zdybska, M Kaniuka, L Molodan, ... | 1 | 2014 |
| Early diagnostic and surgical correction of cjngenital hydronephrosis in children V Davidenko, E Grechanina, V Lapshin, N Roy, T Mayboroda | | 2020 |
| Study of the character of psychiatric symptoms with hereditary metabolic diseases. Symptom complex and comorbidity E Grechanina, Y Grechanina, L Molodan, D Oleinyk, A Zabelina EUROPEAN JOURNAL OF HUMAN GENETICS 27, 635-636, 2019 | | 2019 |
| The discoverer of Canavan syndrome gene: how problems of diagnosis and treatment are being changed over time E Grechanina, J Grechanina, R Matalon, L Delgado, S Tyring Український інститут клінічної генетики ХНМУ, 2019 | | 2019 |
| Shereshevsky-Turner Syndrome: Guidelines for the training of interns, 5th year students E Grechanina, J Grechanina, L Molodan, O Zdybskaya, O Bugaeva, ... | | 2019 |
| Miscarriage: Guidelines E Grechanina, J Grechanina, L Molodan, O Zdybskaya, O Bugaeva, ... | | 2019 |
| Porphyria: Guidelines for the training of interns, 5th year students E Grechanina, J Grechanina, L Molodan, O Zdybskaya, O Bugaeva, ... | | 2019 |
| The case of the combination of limb-girdle myopathy type 2 A with of connective tissue metabolism disorder, hyperhomocysteinemia L Molodan, E Grechanina, Y Grechanina, A Yanovska, K Nagieva EUROPEAN JOURNAL OF HUMAN GENETICS 26, 949-949, 2018 | | 2018 |
| Studying influence of mtDNA polymorphisms and polymorphic gene variants C677T MTHFR and A66G MTRR on clinical manifestations of mitochondrial dysfunction YB Grechanina Клінічна генетика і перинатальна діагностика, 3-22, 2018 | | 2018 |
| AMINO ACIDS IN THE PATHOGENESIS OF PERINATAL HYPOXIC-ISCHEMIC ENCEPHALOPATHY AA Yanovska, EY Grechanina, YB Grechanina Тернопільський державний медичний університет ім. ІЯ Горбачевського, 2017 | | 2017 |
| Selective screening of mitochondrial dysfunction in a region with a high level of neurological diseases E Grechanina, J Grechanina | | 2017 |
| A rare disease of the mitochondrial respiratory chain–3-methylglutaconic aciduria. Approach to diagnosis and rehabilitation E Grechanina, J Grechanina, S Biletska, I Maksutina | | 2017 |
| Амінокислоти крові та органічні кислоти сечі у визначенні метаболічного статусу при перинатальному гіпоксично-ішемічному ураженні ГО Яновська, ОЯ Гречаніна, ЮБ Гречаніна Неонатологія, хірургія та перинатальна медицина, 5-11, 2017 | | 2017 |
| Case of the combination of cystic fibrosis with metabolic disorders of fatty acids and sulfur containing amino acids A Yanovska, J Grechanina, E Grechanina, E Zdybskaya | | 2014 |
| A new variant of Ehlers-Danlos syndrome with inborn errors of mucopolysaccharide metabolism in the mother and son O Bugaeva, E Grechanina, J Grechanina | | 2014 |
| Medical genetics. Сontents module 6. Мitochondrial diseases E Grechanina, J Grechanina, L Molodan, E Zdubskaya, O Bugaeva, ... | | 2013 |
| Medical genetics. Contents module 4. Monogenic diseases. Cystic fibrosis (clinical pictures, diagnosis, treatment) E Grechanina, J Grechanina, L Molodan, E Zdubskaya, O Bugaeva | | 2013 |
| Monogenic diseases. Inherent diseases of CNS E Grechanina, J Grechanina, LV Molodan, EP Zdubskaya, O Bugaeva | | 2013 |
| Medical genetics. Contents module 4. Monogenic diseases. Disorders of amino acid metabolism E Grechanina, J Grechanina, LV Molodan, EP Zdubskaya, O Bugaeva Kharkiv National Medical University, 2013 | | 2013 |
Nataliya Balatska - Балацька Наталія...associate professor of pediatrics department № 1 Bogomolets National Medical UniversityVerified email at kmu.edu.ua
