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Alexander Pakhomov

Observed names: A. P. Pakhomov, A. Pakhomov, A.P. Pakhomo, A.P. Pakhomov, Pakhomov Alexander, А.В. Пахомов, Пахомов Антон Павлович
ORCID: 0000-0002-4686-3245
Observed ORCID: 0000-0002-4686-3245
OpenAlex ID: A5101465716
Bacterial Etiology of Acute Otitis Media and Characterization of Pneumococcal Serotypes and Genotypes among Children in Moscow, Russia
2014 · Nikolay Mayanskiy, Natalia Alyabieva, et al. · The Pediatric Infectious Disease Journal · 20
The prevalence of Fabry disease among 1009 unrelated patients with hypertrophic cardiomyopathy: a Russian nationwide screening program using NGS technology
2022 · K. Savostyanov, A. Pushkov, et al. · Orphanet Journal of Rare Diseases · 17
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Genotype–Phenotype Correlations in 293 Russian Patients with Causal Fabry Disease Variants
2023 · Kirill Savostyanov, Alexander Pushkov, et al. · Genes · 5
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Hypophosphatasia: literature review and description of a clinical case of familial disease with molecular genetic verification of the diagnosis
2023 · E.Yu. Belyashova, A.L. Frolenko, et al. · Лечащий врач · 2
Lyso-Gb3 is as a primary biomarker for Fabry disease screening among high-risk contingents
2019 · Kirill Savostyanov, Alexander Pushkov, et al. · Molecular Genetics and Metabolism · 1
14 novel mutations of GLA gene as a result of selective Fabry disease screening in Russian Federation
2017 · Leyla Namazova-Baranova, Kirill Savostyanov, et al. · Molecular Genetics and Metabolism · 1
Overlap syndrome: juvenile dermatopolymiositis and juvenile idiopathic arthritis, a polyarticular variant in a 2-year-old child
2026 · A.P. Pakhomo, I.V. Zorin, et al. · Лечащий врач
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A case of hemolytic uremic syndrome in a 2-year-old child with acute intestinal infection of viral and bacterial etiology
2026 · A. P. Pakhomov, I. V. Zorin, et al. · CHILDREN INFECTIONS
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Current understanding of cardiorenal syndrome in children
2026 · A. P. Pakhomov, I. V. Zorin · Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics)
Mucocutaneous lymphonodular syndrome (Kawasaki) in a three-year-old child (the clinical case description)
2025 · A.P. Pakhomov, E.V. Saveleva, et al. · Лечащий врач
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Clinical case of lysosomic acid lipase deficiency — cholesterol ethers accumulation diseases
2022 · E.V. Savelieva, A.P. Pakhomov, et al. · Лечащий врач
Measurement of tripeptidyl peptidase 1 activity as a first level test and as a confirmatory test for the diagnosis of neuronal ceroid lipofuscinosis type 2
2022 · Alexander Pushkov, Zhanin Ilya, et al. · Molecular Genetics and Metabolism
90 The first clinical case of rare form of focal epilepsy caused by the novel mutation in the NPRL3 gene in Russian federation and kazakhstan
2021 · Savostyanov Kirill, Nauryzbayeva Alisa, et al. · Abstracts
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Clinical case of mucopolysaccharidosis type II (Hunter syndrome)
2021 · E. V. Savelieva, A. P. Pakhomov, et al. · Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics)
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RASopathies in multidisciplinary pediatric hospita
2020 · Н.В. Журкова, Л.А. Гандаева, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
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Next generation sequencing is useful for the diagnosis of mucopolysaccharidosis type III in Russian patients
2020 · Alexander Pushkov, Kirill Savostyanov, et al. · Molecular Genetics and Metabolism
Selective screening for nephropathic cystinosis among high-risk contingents of the children population in Russia
2020 · Kirill Savostyanov, Alexander Pushkov, et al. · Molecular Genetics and Metabolism
111 Next generation sequencing is the suitable method for identification of hereditary dermatosis with EB symptom complex in Russian patients
2019 · A. Pushkov, N. Murashkin, et al. · Journal of Investigative Dermatology
OC8 High prevalence ofwt1gene mutations in patients with steroid-resistant nephrotic syndrome
2019 · Dmitry Sladkov, Kirill Savostyanov, et al. · Abstracts
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Случай гемолитико-уремического синдрома у ребёнка 2-х лет с острой кишечной инфекцией вирусно-бактериальной этиологии
· Пахомов Антон Павлович, Зорин Игорь Владимирович, et al. · CyberLeninK (CyberLeninka)
Works count: 20
Citation count: 46
H-index: 3
I10-index: 2
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