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[Statistics of outpatient cases of Parkinson's disease].

Razdorskaia, V V; Iudina, G K; Voskresenskaia, O N.

Zh Nevrol Psikhiatr Im S S Korsakova ; 112(9): 72-6, 2012.

Article in Russian | MEDLINE | ID: mdl-23235417

Subject(s)

Outpatients/statistics & numerical data , Parkinson Disease/epidemiology , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Moscow/epidemiology , Parkinson Disease/diagnosis

[A case of hemiparkinsonism--hemiatrophy syndrome with early onset].

Iudina, V V; Voskresenskaia, O N; Iudina, G K.

Zh Nevrol Psikhiatr Im S S Korsakova ; 110(7): 65-8, 2010.

Article in Russian | MEDLINE | ID: mdl-21465822

Subject(s)

Brain/pathology , Dystonia/diagnosis , Parkinson Disease/diagnosis , Adolescent , Atrophy/diagnosis , Atrophy/diagnostic imaging , Atrophy/physiopathology , Brain/diagnostic imaging , Female , Humans , Parkinson Disease/diagnostic imaging , Parkinson Disease/physiopathology , Radiography , Syndrome

[Clinical genetic characteristics of hereditary extrapyramidal diseases in Saratov region].

Iudina, G K; Solovykh, N N; Sholomov, I I.

Zh Nevrol Psikhiatr Im S S Korsakova ; 105(5): 52-5, 2005.

Article in Russian | MEDLINE | ID: mdl-15952540

Subject(s)

Basal Ganglia Diseases , Chromosomes, Human, Pair 4/genetics , Adolescent , Adult , Basal Ganglia Diseases/epidemiology , Basal Ganglia Diseases/genetics , Basal Ganglia Diseases/physiopathology , Catchment Area, Health , DNA Mutational Analysis , Female , Humans , Male , Middle Aged , Point Mutation/genetics , Prevalence , Russia/epidemiology , Syndrome

[Rare and atypical forms of spinal muscle atrophies in Saratov region].

Iudina, G K; Kolokolov, O V.

Zh Nevrol Psikhiatr Im S S Korsakova ; 105(6): 51-6, 2005.

Article in Russian | MEDLINE | ID: mdl-15986519

Subject(s)

Muscular Atrophy, Spinal/epidemiology , Adult , Aged , Autoantigens , Brain/pathology , Catchment Area, Health , Female , Humans , Male , Middle Aged , Muscular Atrophy, Spinal/genetics , Neuroglia/pathology , Pedigree , Ribonucleoproteins, Small Nuclear/genetics , Russia/epidemiology , snRNP Core Proteins

[Hereditary motosensory neuropathies in Saratov region]. / Nasledstvennye motosensornye nevropatii v Saratovskoi oblasti.

Iudina, G K; Sirkov, E A; Grigor'eva, E A.

Zh Nevrol Psikhiatr Im S S Korsakova ; 104(10): 62-6, 2004.

Article in Russian | MEDLINE | ID: mdl-15553380

Subject(s)

Hereditary Sensory and Autonomic Neuropathies , Adolescent , Adult , Catchment Area, Health , Electromyography , Female , Hereditary Sensory and Autonomic Neuropathies/epidemiology , Hereditary Sensory and Autonomic Neuropathies/genetics , Hereditary Sensory and Autonomic Neuropathies/physiopathology , Humans , Male , Middle Aged , Pedigree , Russia/epidemiology

[A case of spinal muscle atrophy with lesions of hand and thigh muscles]. / Sluchai spinal'noi myshechnoi atrofii s porazheniem myshts beder i kistei.

Iudina, G K; Grigor'eva, E A.

Zh Nevrol Psikhiatr Im S S Korsakova ; 104(9): 58-9, 2004.

Article in Russian | MEDLINE | ID: mdl-15490944

Subject(s)

Muscle, Skeletal/pathology , Adult , Atrophy/classification , Atrophy/pathology , Hand , Humans , Male , Motor Neurons/pathology , Spinal Cord/pathology , Spine , Terminology as Topic , Thigh

[Proximal autosomal recessive types of spinal muscular atrophy]. / Proksimal'nye autosomno-retsessivnye formy spinal'noi myshechnoi atrofii.

Kolokolov, O V; Iudina, G K; Solovykh, N N; Evgrafov, O V.

Zh Nevrol Psikhiatr Im S S Korsakova ; 103(8): 66-8, 2003.

Article in Russian | MEDLINE | ID: mdl-14564781

ABSTRACT

One hundred and three patients with spinal muscular atrophy (SMA) were registered in a population medical genetic study of autosomal recessive childhood proximal SMA in Saratov region. Twenty-five patients were investigated complexly, using biochemical analysis of some enzymes, electroneuromyography, magnetic resonance imaging of spinal cord, muscle biopsy and molecular genetic testing. Pronounced clinical polymorphism and genetic heterogeneity of the disease were revealed.

Subject(s)

Chromosomes, Human, Pair 5/genetics , Nerve Tissue Proteins/genetics , Spinal Muscular Atrophies of Childhood/genetics , Biopsy , Child , Cyclic AMP Response Element-Binding Protein , Female , Humans , Magnetic Resonance Imaging , Male , Muscle, Skeletal/pathology , Point Mutation/genetics , RNA-Binding Proteins , SMN Complex Proteins , Spinal Cord/pathology , Spinal Muscular Atrophies of Childhood/diagnosis

[A familial case of Hallervorden-Spatz disease]. / Semeinyi sluchai bolezni Gallervordena-Shpatsa.

Iudina, G K; Sholomov, I I.

Zh Nevrol Psikhiatr Im S S Korsakova ; 103(1): 49-50, 2003.

Article in Russian | MEDLINE | ID: mdl-12616740

Subject(s)

Pantothenate Kinase-Associated Neurodegeneration/genetics , Adolescent , Anticonvulsants/therapeutic use , Carbamazepine/therapeutic use , Diagnosis, Differential , Female , Humans , Pantothenate Kinase-Associated Neurodegeneration/diagnosis , Pantothenate Kinase-Associated Neurodegeneration/drug therapy

[Extrauterine pregnancy]. / Vnematochnaia beremennost'.

Martynova, N V; Iudina, G K.

Vopr Okhr Materin Det ; 15(5): 87-8, 1970 May.

Article in Russian | MEDLINE | ID: mdl-5464365

Subject(s)

Pregnancy, Ectopic , Adult , Female , Humans , Pregnancy

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