CONNECTIVE TISSUE DYSPLASIA AS A CAUSE OF CHRONIC CONSTIPATION IN CHILDREN by E.V. Komarova, A.S. Potapov, N.V. Zhurkova, O.B. Kondakova

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CONNECTIVE TISSUE DYSPLASIA AS A CAUSE OF CHRONIC CONSTIPATION IN CHILDREN by E.V. Komarova, A.S. Potapov, N.V. Zhurkova, O.B. Kondakova

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CLINIC, DIFFERENTIAL DIAGNOSIS AND TREATMENT OF GALACTOSEMIA by N.V. Zhurkova, O.B. Kondakova, T.V. Bushueva, E.P. Rybakova, T.E. Borovik

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CLINIC, DIFFERENTIAL DIAGNOSIS AND TREATMENT OF GALACTOSEMIA by N.V. Zhurkova, O.B. Kondakova, T.V. Bushueva, E.P. Rybakova, T.E. Borovik

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Type 6 hypomyelinating leukodystrophy caused by a de novo mutation in the tubulin beta-4A gene by I. Yu. Ozhegova, A. Yu. Asanov, O. N. Voskresenskaya, D. S. Razheva, O. B. Kondakova, E. A. Nikolaeva

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A CASE OF PERSISTANT INTRACRANIAL HYPERTENSION IN A 7 YEARS OLD GIRL WITH MULTIPLE HEREDITARY EXOSTOSIS AND CRANIOSTENOSIS by L.M. Kuzenkova, E.M. Mazurina, O.B. Kondakova, N.V. Zhurkova, O.V. Chumakova, I.M. Abdraziakova

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A CASE OF PERSISTANT INTRACRANIAL HYPERTENSION IN A 7 YEARS OLD GIRL WITH MULTIPLE HEREDITARY EXOSTOSIS AND CRANIOSTENOSIS by L.M. Kuzenkova, E.M. Mazurina, O.B. Kondakova, N.V. Zhurkova, O.V. Chumakova, I.M. Abdraziakova

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A CLINICAL CASE: DIAGNOSTICS OF SHERESHEVSKY TERNER SYNDROME WITH MULTIPLE CONGENITAL ANOMALIES IN MAIN ARTERIES OF A 4 YEAR OLD CHILD, SUFFERING FROM ARTERIAL HYPERTENSION by A.N. Tsygin, A.N. Sikachev, N.N. Kartamysheva, E.N. Tsygina, Z.P. Sharnova, O.B. Kondakova, N.V. Zhurkova

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A CLINICAL CASE: DIAGNOSTICS OF SHERESHEVSKY TERNER SYNDROME WITH MULTIPLE CONGENITAL ANOMALIES IN MAIN ARTERIES OF A 4 YEAR OLD CHILD, SUFFERING FROM ARTERIAL HYPERTENSION by A.N. Tsygin, A.N. Sikachev, N.N. Kartamysheva, E.N. Tsygina, Z.P. Sharnova, O.B. Kondakova, N.V. Zhurkova

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A new nucleotide variant in the <I>ELAC2</I> gene in a young child with a ventricular hypertrophy by L. A. Gandaeva, E. N. Basargina, O. B. Kondakova, V. G. Kaverina, A. A. Pushkov, O. P. Zharova, P. P. Fisenko, K. V. Savostyanov

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Glycogen storage disease: PRKAG2 syndrome by L.  A.  Gandaeva, O. B. Kondakova, E. N. Basargina, A. A. Pushkov, N. N. Koloskova, O. P. Zharova, V. I. Barsky, A. P. Fisenko, K. V. Savostyanov

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Family case of aromatic L-amino acid decarboxylase deficiency by O. B. Kondakova, K. A. Kazakova, A. A. Lyalina, N. V. Lapshina, A. A. Pushkov, N. N. Mazanova, Yu. I. Davydova, D. I. Grebenkin, I. V. Kanivets, K. V. Savostyanov

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