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878 results on '"Ataxia complications"'

801. Angelman's ("happy puppet") syndrome.

Author

Berg JM and Pakula Z

Subjects
Abnormalities, Multiple, Child, Dermatoglyphics, Electroencephalography, Female, Gait, Humans, Laughter, Microcephaly complications, Prognathism, Salivation, Tongue Habits, Ataxia complications, Epilepsy complications, Intellectual Disability complications
Published
1972
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802. Hereditary deafness in man.

Author

Konigsmark BW

Subjects
Abnormalities, Multiple, Adult, Ataxia complications, Bone and Bones abnormalities, Cataract complications, Child, Child, Preschool, Deafness congenital, Diabetes Complications, Diabetes Mellitus, Type 1 complications, Diabetic Neuropathies complications, Diabetic Retinopathy complications, Gait, Genes, Dominant, Genes, Recessive, Humans, Hypogonadism complications, Intellectual Disability complications, Kidney Diseases complications, Middle Aged, Muscular Diseases complications, Myoclonus complications, Myopia complications, Neurilemmoma complications, Nose Deformities, Acquired complications, Obesity complications, Optic Atrophy complications, Peripheral Nervous System Diseases complications, Refsum Disease genetics, Retinitis Pigmentosa complications, Vestibulocochlear Nerve, Deafness complications, Deafness genetics, Eye Diseases complications, Nervous System Diseases complications
Published
1969
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804. Ataxia and myxoedema.

Subjects
Ataxia diagnosis, Humans, Myxedema diagnosis, Ataxia complications, Myxedema complications
Published
1967

805. Progressive ataxia of Charolais cattle associated with a myelin disorder.

Author

Palmer AC, Blakemore WF, Barlow RM, Fraser JA, and Ogden AL

Subjects
Animals, Ataxia complications, Cattle, Eosinophils, Female, France, Hypodermyiasis veterinary, Lymph Nodes pathology, Microscopy veterinary, Microscopy, Electron veterinary, Myelitis complications, United Kingdom, Urinary Incontinence veterinary, Ataxia veterinary, Cattle Diseases, Myelitis veterinary
Published
1972
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806. Lesions associated with the developing of ataxia in vitamin A-deficient chicks.

Author

Howell MC and Thompson JN

Subjects
Animals, Cartilage growth & development, Chickens growth & development, Epiphyses growth & development, Male, Metaplasia, Nerve Degeneration, Osteoblasts growth & development, Ataxia complications, Bone Development, Bone and Bones pathology, Central Nervous System growth & development, Central Nervous System pathology, Nasal Mucosa pathology, Vitamin A Deficiency complications
Published
1967
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807. [Ataxia in mumps].

Author

SEDALLIAN P, GARIN JP, FAYOLLE J, and MARIN A

Subjects
Humans, Ataxia complications, Mumps complications
Published
1957

808. Clinical manifestations of essential tremor.

Author

Critchley E

Subjects
Adult, Aged, Amantadine therapeutic use, Ataxia complications, Chlordiazepoxide therapeutic use, Dihydroxyphenylalanine therapeutic use, Female, Humans, Male, Mephenesin therapeutic use, Middle Aged, Movement Disorders complications, Nerve Degeneration, Parkinson Disease drug therapy, Sweating, Tremor complications, Tremor drug therapy, Tremor genetics
Abstract

A clinical study of 42 patients with essential tremor is presented. In the case of 12 patients the family history strongly suggested an autosomal dominant mode of transmission, in four the mode of inheritance was indeterminate, and the remaining 26 patients were sporadic cases without an established genetic basis. The tremor involved the upper extremities in 41 patients, the head in 25, lower limbs in 15, and trunk in two. Seven patients showed involvement of speech. Variations were found in the speed and regularity of the tremor. Leg involvement took a variety of forms: (1) direct involvement by tremor; (2) a painful limp associated with forearm tremor; (3) associated dyskinetic movements; (4) ataxia; (5) foot clubbing; and (6) evidence of peroneal muscular atrophy. Several minor symptoms-hyperhidrosis, cramps, dyskinetic movements, and ataxia-were associated with essential tremor. Other features were linked phenotypically to the ataxias and system degenerations. Apart from minor alterations in tone, expression, and arm swing, features of Parkinsonism were notably absent.

Published
1972
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809. Progressive supranuclear palsy. Report of a Thai patient.

Author

Steele JC

Subjects
Humans, Male, Middle Aged, Thailand, Ataxia complications, Bulbar Palsy, Progressive complications, Deglutition Disorders complications, Dementia complications, Vision Disorders complications
Published
1970

812. The night-blinding disorders.

Author

Carr RE

Subjects
Abnormalities, Multiple complications, Ataxia complications, Blood Protein Disorders complications, Carbohydrate Metabolism, Inborn Errors complications, Chromosome Aberrations, Chromosome Disorders, Chromosomes, Human, 6-12 and X, Diagnosis, Differential, Dwarfism complications, Electrooculography, Electroretinography, Glycosaminoglycans metabolism, Growth Disorders complications, Humans, Ichthyosis complications, Intellectual Disability complications, Laurence-Moon Syndrome complications, Lipid Metabolism, Inborn Errors complications, Lipidoses complications, Lipids blood, Lipoproteins blood, Muscle Spasticity complications, Muscular Dystrophies complications, Night Blindness congenital, Night Blindness etiology, Ophthalmoplegia complications, Refsum Disease complications, Retinal Degeneration complications, Retinitis Pigmentosa complications, Trisomy, Vision Disorders congenital, Vitamin A Deficiency complications, Eye Diseases complications, Night Blindness diagnosis
Published
1969
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813. Hereditary olivopontocerebellar atrophy with retinal degeneration. Report of a family through six generations.

Author

Weiner LP, Konigsmark BW, Stoll J Jr, and Magladery JW

Subjects
Adolescent, Adult, Aged, Ataxia complications, Athetosis complications, Blindness complications, Cerebellar Cortex pathology, Child, Female, Humans, Male, Medulla Oblongata pathology, Middle Aged, Neurons pathology, Purkinje Cells pathology, Retina pathology, Speech Disorders complications, Substantia Nigra pathology, Atrophy genetics, Brain Diseases genetics, Cerebellum pathology, Olivary Nucleus pathology, Pons pathology, Retinitis Pigmentosa complications
Published
1967
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814. Bilateral optic atrophy in childhood. II.

Author

Harcourt B and Jay B

Subjects
Ataxia complications, Cerebral Palsy complications, Child, Craniocerebral Trauma complications, Diffuse Cerebral Sclerosis of Schilder complications, Encephalomyelitis complications, Humans, Hydrocephalus complications, Lipidoses complications, Meningitis complications, Microcephaly complications, Syphilis, Congenital complications, Optic Atrophy etiology
Published
1968
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815. Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia. A unique and partially treatable clinico-pathological entity.

Author

Woods BT and Schaumburg HH

Subjects
Adult, Aged, Ataxia genetics, Ataxia pathology, Basal Ganglia Diseases complications, Basal Ganglia Diseases genetics, Cerebellar Diseases genetics, Cerebellar Diseases pathology, Cerebellar Nuclei pathology, Female, Genes, Dominant, Humans, Male, Middle Aged, Oculomotor Nerve pathology, Ophthalmoplegia genetics, Ophthalmoplegia pathology, Pedigree, Spinal Cord pathology, Spinal Cord Diseases genetics, Spinal Cord Diseases pathology, Substantia Nigra pathology, Tegmentum Mesencephali pathology, Ataxia complications, Cerebellar Diseases complications, Nerve Degeneration, Ophthalmoplegia complications, Spinal Cord Diseases complications
Published
1972
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816. Biochemical studies in Tanzanian patients with ataxic tropical neuropathy.

Author

Makene WJ and Wilson J

Subjects
Ataxia complications, Humans, Mental Disorders complications, Nervous System Diseases chemically induced, Nervous System Diseases complications, Optic Atrophy complications, Tanzania, Ataxia blood, Cyanides poisoning, Manihot, Nervous System Diseases blood, Thiocyanates blood, Vitamin B 12 blood
Abstract

Data on thiocyanate and vitamin B(12) concentrations in plasma from Tanzanian patients with ataxic tropical neuropathy are presented and support the hypothesis that, as in Nigeria, the condition may result from chronic exposure to cyanide or cyanogens from a diet including large amounts of cassava.

Published
1972
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818. [Syndrome of myatrophic ataxia].

Author

Lange E, Kulawik H, and Kunath B

Subjects
Ataxia diagnosis, Ataxia pathology, Biopsy, Diagnosis, Differential, Electromyography, Friedreich Ataxia complications, Friedreich Ataxia diagnosis, Humans, Male, Middle Aged, Muscular Atrophy diagnosis, Muscular Atrophy pathology, Myelography, Peripheral Nerves pathology, Phlebography, Radionuclide Imaging, Syndrome, Ataxia complications, Muscular Atrophy complications
Published
1972

819. Orthopaedic problems associated with tuberous sclerosis.

Author

Smith TK, Gregersen GG, and Samilson RL

Subjects
Achilles Tendon surgery, Adolescent, Adult, Ankle surgery, Ataxia complications, Cerebral Palsy etiology, Child, Clubfoot etiology, Contracture etiology, Elbow surgery, Female, Foot diagnostic imaging, Foot surgery, Foot Deformities, Congenital, Fractures, Bone etiology, Hand diagnostic imaging, Hip, Humans, Ilium diagnostic imaging, Joint Dislocations etiology, Knee, Male, Paraplegia etiology, Quadriplegia etiology, Radiography, Scoliosis etiology, Shoulder, Skull diagnostic imaging, Tibial Fractures diagnostic imaging, Tibial Fractures etiology, Tuberous Sclerosis diagnostic imaging, Bone Diseases etiology, Tuberous Sclerosis complications
Published
1969

821. Congenital adrenal hyperplasia. Report of a case with neurological complications.

Author

Hanefeld F, Crome L, France NE, and Jackson AD

Subjects
Adrenal Hyperplasia, Congenital drug therapy, Adrenal Hyperplasia, Congenital pathology, Ataxia complications, Atrophy complications, Brain pathology, Brain Diseases complications, Cerebellum pathology, Cerebral Cortex pathology, Cortisone therapeutic use, Desoxycorticosterone therapeutic use, Diffuse Cerebral Sclerosis of Schilder complications, Female, Humans, Infant, Myoclonus complications, Occipital Lobe pathology, Organ Size, Sodium Chloride therapeutic use, Adrenal Hyperplasia, Congenital complications, Neurologic Manifestations
Published
1973
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822. Experimental cerebellar uvulonodular lesions in the squirrel monkey.

Author

Igarashi M, Miyata H, Alford BR, and Wright WK

Subjects
Animals, Ataxia complications, Brain Stem physiology, Computers, Electrooculography, Eye Movements, Kinetics, Nerve Tissue physiology, Postural Balance, Posture, Reflex, Rotation, Synaptic Transmission, Temporal Bone physiology, Time Factors, Vestibular Function Tests, Cerebellum physiology, Haplorhini physiology
Published
1973
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823. Genetic approach to the nosology of retinal disorders.

Author

Klein D

Subjects
Abnormalities, Multiple complications, Adolescent, Adult, Ataxia complications, Atrophy, Blindness genetics, Choroid, Eye Diseases genetics, Female, Humans, Infant, Macular Degeneration genetics, Male, Metabolism, Inborn Errors complications, Middle Aged, Pedigree, Retinal Degeneration classification, Retinitis congenital, Retinitis Pigmentosa genetics, Syndrome, Vision Disorders congenital, Vitreous Body, Retinal Degeneration genetics
Abstract

During the last 20 years we have carried out, with the collaborators of our Institute, a series of genetic and epidemiologic investigations on tapetoretinal degenerations and allied diseases in Switzerland. Basing conclusions both on the results of this inquiry and on the findings in the literature, we give in this study a general survey of the chorioretinal abiotrophies and describe in particular their clinical and genetic aspects as well as their association with other congenital and hereditary anomalies. A nosologic classification is proposed which takes into account the clinical and genetic features of the systemic heredodegenerative conditions of the retina.

Published
1971

824. Dominant spino-pontine atrophy. Report of a family through three generations.

Author

Taniguchi R and Konigsmark BW

Subjects
Adult, Ataxia classification, Ataxia complications, Ataxia diagnosis, Ataxia pathology, Atrophy genetics, Autopsy, Black People, Cerebellar Ataxia diagnosis, Cerebellum pathology, Diagnosis, Differential, Female, Genes, Dominant, Humans, Male, Middle Aged, Nystagmus, Pathologic etiology, Olivary Nucleus pathology, Pedigree, Reflex, Abnormal etiology, Sensory Deprivation etiology, Speech Disorders etiology, Spinal Cord pathology, Spinal Diseases diagnosis, Ataxia genetics, Pons pathology, Spinal Cord Diseases genetics
Published
1971
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826. Progressive ataxia, retinal degeneration, neuromyopathy, and mental subnormality in a patient with true hypoparathyroidism, dwarfism, malabsorption, and cholelithiasis.

Author

Gomez MR, Engel AG, and Dyck PJ

Subjects
Adult, Female, Hepatomegaly complications, Humans, Metabolism, Inborn Errors complications, Microscopy, Electron, Muscles pathology, Neuromuscular Diseases pathology, Scoliosis complications, Splenomegaly complications, Vestibulocochlear Nerve, Ataxia complications, Cholelithiasis complications, Dwarfism complications, Hypoparathyroidism complications, Intellectual Disability complications, Malabsorption Syndromes complications, Neuromuscular Diseases complications, Retinal Degeneration complications
Published
1972
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827. A neurological note on vaccination against influenza.

Author

Wells CE

Subjects
Adolescent, Adult, Ataxia complications, Back Pain complications, Child, Constipation complications, Electroencephalography, Female, Hemagglutination Inhibition Tests, Humans, Male, Middle Aged, Neurologic Manifestations, Visual Acuity drug effects, Influenza Vaccines adverse effects, Paralysis etiology, Vision Disorders etiology
Abstract

Vaccination against influenza may be complicated by a neurological illness. Two case histories are presented together with a summary of seven others.

Published
1971
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828. Hearing levels in Nigerian ataxic neuropathy.

Author

Hinchcliffe R, Osuntokun BO, and Adeuja AO

Subjects
Adolescent, Adult, Audiometry, Auditory Threshold, Cyanides poisoning, Female, Hearing Disorders complications, Humans, Male, Manihot, Nervous System Diseases complications, Nigeria, Peripheral Nervous System Diseases complications, Spinal Cord Diseases complications, Syndrome, Ataxia complications, Hearing Disorders diagnosis
Published
1972
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829. [Ataxia associated with autonomic nerve diseases].

Author

Takahashi A

Subjects
Adult, Ataxia genetics, Cerebellar Ataxia complications, Cerebellar Diseases complications, Fecal Incontinence complications, Female, Humans, Hypotension, Orthostatic complications, Male, Middle Aged, Nervous System Diseases complications, Ophthalmoplegia complications, Pedigree, Urinary Bladder, Neurogenic complications, Urinary Incontinence complications, Ataxia complications, Autonomic Nervous System
Published
1971

830. Myxedema and ataxia.

Author

Cremer GM, Paris J, and Goldstein NP

Subjects
Ataxia complications, Ataxia etiology, Cerebellar Ataxia diagnosis, Cerebellar Ataxia drug therapy, Hormones therapeutic use, Humans, Hypothyroidism etiology, Myxedema diagnosis, Neurologic Manifestations, Cerebellar Ataxia complications, Myxedema complications
Published
1968

831. Argininosuccinic aciduria. Case report with neuropathological findings.

Author

Lewis PD and Miller AL

Subjects
Adolescent, Amino Acid Metabolism, Inborn Errors complications, Ataxia complications, Autopsy, Brain pathology, Cerebral Cortex pathology, Epilepsy complications, Humans, Intellectual Disability complications, Liver enzymology, Lyases analysis, Male, Pedigree, Sleep Wake Disorders complications, Thalamus pathology, Amino Acid Metabolism, Inborn Errors pathology, Arginine urine, Succinates urine
Published
1970
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832. Familial intention tremor, ataxia, and lipofuscinosis. Liver biopsy studies.

Author

Feldman RG, Iseri OA, Gottlieb LS, and Greenberg JP

Subjects
Adult, Ataxia complications, Biopsy, Child, Chromatophores, Female, Gait, Humans, Lipid Metabolism, Lysosomes, Male, Middle Aged, Olivary Nucleus, Pedigree, Pigmentation Disorders complications, Tremor complications, Ataxia genetics, Liver pathology, Pigmentation Disorders genetics, Tremor genetics
Published
1969
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833. Erythrokeratodermia with ataxia.

Author

Giroux JM and Barbeau A

Subjects
Adult, Aged, Ataxia genetics, Biopsy, Female, Humans, Lipids blood, Male, Pedigree, Skin pathology, Skin Diseases complications, Skin Diseases pathology, Syndrome, Ataxia complications, Skin Diseases genetics
Published
1972

835. Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus.

Author

Young GF, Leon-Barth CA, and Green J

Subjects
Female, Humans, Male, Adult, Ataxia complications, Ataxia genetics, Child, Preschool, Chromosome Aberrations, Chromosome Disorders, Deafness complications, Deafness genetics, Electroencephalography, Epilepsy genetics, Gait, Hemiplegia complications, Hemiplegia genetics, Migraine Disorders complications, Migraine Disorders genetics, Nervous System Diseases complications, Night Blindness, Nystagmus, Pathologic complications, Nystagmus, Pathologic genetics, Pedigree, Retinal Degeneration genetics, Retinitis Pigmentosa complications, Retinitis Pigmentosa genetics
Published
1970
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836. Allergic encephalomyelitis in monkeys induced with A-1 protein.

Author

Jackson JJ, Brostoff SW, Lampert P, and Eylar EH

Subjects
Animals, Ataxia complications, Brain pathology, Cattle, Desensitization, Immunologic, Encephalomyelitis, Autoimmune, Experimental complications, Encephalomyelitis, Autoimmune, Experimental pathology, Feeding and Eating Disorders complications, Female, Haplorhini, Humans, Leukocytes, Macaca, Male, Meninges pathology, Muscular Diseases complications, Myelin Basic Protein isolation & purification, Neutrophils, Rabbits, Species Specificity, Spinal Cord pathology, Encephalomyelitis, Autoimmune, Experimental chemically induced, Nerve Tissue Proteins
Published
1972

837. G5-ganglioside variant of systemic late infantile lipidosis. Generalized gangliosidosis.

Author

Volk BW, Adachi M, Schneck L, Saifer A, and Kleinberg W

Subjects
Ataxia complications, Biopsy, Brain pathology, Brain Chemistry, Cerebellum analysis, Cerebral Cortex analysis, Cerebral Cortex pathology, Child, Chromatography, Thin Layer, Gangliosides analysis, Histocytochemistry, Humans, Lipidoses metabolism, Lipids analysis, Liver analysis, Liver pathology, Male, Microscopy, Electron, Myocardium analysis, Neuroglia, Neurons, Psychomotor Disorders complications, Lipidoses pathology
Published
1969

838. Immunological deficiency and malignant lymphoma.

Author

Miller DG

Subjects
Anemia, Hemolytic, Autoimmune etiology, Ataxia complications, Autoimmune Diseases complications, Hodgkin Disease immunology, Humans, Leukemia, Lymphoid immunology, Lymphocytes, Sjogren's Syndrome complications, Thymus Gland physiopathology, Lymphoma complications, Lymphoma immunology
Published
1967
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839. Progressive ophthalmoplegia. Report of cases.

Author

Rosenberg RN, Schotland DL, Lovelace RE, and Rowland LP

Subjects
Abetalipoproteinemia complications, Adolescent, Adult, Age Factors, Aged, Ataxia complications, Blepharoptosis, Dystonia Musculorum Deformans complications, Electromyography, Female, Humans, Intellectual Disability complications, Male, Middle Aged, Ophthalmoplegia complications, Paraplegia complications, Peripheral Nervous System Diseases complications, Refsum Disease complications, Retinitis Pigmentosa complications, Seizures complications, Oculomotor Muscles physiopathology, Oculomotor Nerve physiopathology, Ophthalmoplegia physiopathology
Published
1968
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840. Neuromotor pathologies of speech.

Author

Canter GJ

Subjects
Ataxia complications, Central Nervous System Diseases complications, Facial Paralysis complications, Humans, Hypoglossal Nerve pathology, Motor Neurons pathology, Movement Disorders complications, Muscular Dystrophies complications, Myasthenia Gravis complications, Palate pathology, Paralysis, Spasm complications, Vocal Cord Paralysis complications, Speech Disorders etiology
Published
1967

841. [Change from athrombone to chlorathrombone].

Author

Geidel H and Helbig A

Subjects
Arrhythmias, Cardiac complications, Ataxia complications, Female, Humans, Male, Phenindione adverse effects, Thrombophlebitis prevention & control, Anticoagulants administration & dosage, Myocardial Infarction drug therapy, Phenindione administration & dosage, Pulmonary Embolism drug therapy
Published
1966

842. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.

Author

Shih VE, Efron ML, and Moser HW

Subjects
Amino Acid Metabolism, Inborn Errors blood, Amino Acid Metabolism, Inborn Errors complications, Amino Acid Metabolism, Inborn Errors enzymology, Amino Acid Metabolism, Inborn Errors genetics, Amino Acid Metabolism, Inborn Errors therapy, Amino Acid Metabolism, Inborn Errors urine, Amino Acids blood, Ataxia complications, Child, Preschool, Diet Therapy, Humans, Lysine metabolism, Male, Ornithine metabolism, Ornithine Carbamoyltransferase metabolism, Seizures complications, Amino Acid Metabolism, Inborn Errors metabolism, Ammonia blood, Citrulline urine, Intellectual Disability complications, Myoclonus complications, Ornithine blood
Published
1969

843. Benedict's syndrome. Report of a case in infancy.

Author

Pingle P and Belapurker KM

Subjects
Ataxia complications, Child, Preschool, Humans, Male, Mesencephalon physiopathology, Paralysis complications, Tremor complications, Hyperkinesis complications, Ophthalmoplegia complications, Vestibular Nuclei physiopathology
Published
1969
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844. Subacute necrotizing encephalomyelopathy associated with renal and arterial lesions.

Author

Crome L

Subjects
Arteries pathology, Ataxia complications, Autopsy, Basal Ganglia pathology, Carotid Artery Diseases complications, Encephalomalacia pathology, Encephalomyelitis pathology, Humans, Infant, Intellectual Disability complications, Male, Psychomotor Disorders complications, Seizures complications, Substantia Nigra pathology, Thalamus pathology, Acidosis complications, Acute Kidney Injury complications, Brain Stem pathology, Encephalomalacia complications, Encephalomyelitis complications, Vascular Diseases complications
Published
1970
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845. Achilles tenoplasty for correction of equinus deformity in spastic syndromes of cerebral palsy.

Author

Lemperg R, Hagberg B, and Lundberg A

Subjects
Adolescent, Ataxia complications, Child, Child, Preschool, Clubfoot complications, Exercise Therapy, Follow-Up Studies, Gait, Hemiplegia complications, Humans, Male, Movement Disorders complications, Muscles surgery, Postoperative Care, Achilles Tendon surgery, Cerebral Palsy complications, Clubfoot surgery
Published
1969
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848. [Ataxia teleangiectatica (Louis-Bar syndrome)].

Author

SCHEDA W and SZARVASSY G

Subjects
Ataxia complications, Ataxia Telangiectasia, Bronchiectasis, Cerebellar Diseases, Cerebellum, Conjunctiva, Disease, Telangiectasis
Published
1961

850. Familial periodic nystagmus, vertigo, and ataxia.

Author

White JC

Subjects
Adult, Ataxia complications, Child, Female, Humans, Infant, Infant, Newborn, Male, Middle Aged, Nystagmus, Pathologic complications, Pedigree, Vertigo complications, Ataxia genetics, Nystagmus, Pathologic genetics, Vertigo genetics
Published
1969
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