Disease: Oligophernia
- A case of generalized convulsion during induction with Diprivan
- A mathematical model of the behavior formation in mastering the determinate patterns of stimuli
- Amniotic membrane transplantation with cauterization for keratoconus complicated by persistent hydrops in mentally retarded patients
- An unusual type of primary cerebral hemihypotrophy with signs of dysfunctional neuronal migration
- Binder syndrome: Clinical findings and surgical treatment of 18 patients at the Department of Plastic Surgery in Polanica Zdrój
- Catamnestic study of children hospitalized with the diagnosis of Kanner's infantile autism
- Cerebellar cognitive affective syndrome without global mental retardation in two relatives with Gillespie syndrome
- Cerebellar vermis defect, oligophrenia, congenital ataxia, and hepatic fibrocirrhosis without coloboma and renal abnormalities: report of three cases
- Characteristics of hormonal homeostasis in adolescents with mental disorders
- Children's Doctor Games and Nudity at Danish Childcare Institutions
- Chorioretinal lesions in deaf mutes
- Chotzen-Saethre syndrome with oligophrenia and psychological abnormal development
- Classifying the women: psychiatric diagnoses and female subjectivity in the Manicomio Provincial de Málaga, Spain, 1909-1950
- Clinical and cytogenetic diagnosis of Martin-Bell syndrome
- Clinical features and revised diagnostic criteria in Joubert syndrome
- Clinical manifestations of oligophrenia with fragile X syndrome in boys in the pre- and post-pubertal age
- Clinical nosologic and genetic aspects of Joubert and related syndromes
- Clinical presentations and a classification of oligophrenia psychoses in children
- Clinico-electrophysiological study of behavior disorders in children with oligophrenia
- COACH syndrome associated with multifocal liver tumors
- COACH syndrome: report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation
- Comparative studies of hearing in children by recording reflex reactions and long-latency auditory evoked potentials
- Congenital cataract associated with mental retardation and epilepsy
- Could the complications of megacolon be avoided by monitoring the risk patients? cases report
- De Sanctis-Caccione syndrome: xeroderma pigmentosum with oligophrenia, short stature and neurologic disorders
- Dealing with congenital hepatic fibrosis? Remember COACH syndrome
- Dynamics of mental disorders after extracerebral implantation of embryonal nervous tissue in epilepsy
- Early detection of severe cholestatic hepatopathy in COACH syndrome
- Effect of psychiatric service resources on detection of mentally ill patients in Siberia and Far East (correlation-regression analysis)
- Endogenous psychoses and consanguinity (among an isolated population)
- Epileptic fit: the most dramatic sign of tuberous sclerosis
- Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome
- Further delineation of a syndrome of cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, coloboma, and hepatic fibrosis
- Genetics of syndromic ocular coloboma: CHARGE and COACH syndromes
- German neurology and neurologists during the Third Reich: brain research and "euthanasia"
- Gingival fibromatosis with oligophrenia and self-injurious behavior
- GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible "new" recessively inherited MCA/MR syndrome
- Herpetic Esophagitis: A Cause of Dysphagia in a Malnourished Patient
- High-resolution cytogenetic analysis of the peripheral blood lymphocytes of patients with autosomal dominant polycystic kidney disease
- Hyperlipoproteinemia in mentally retarded children
- Hypertrophic cardiomyopathy occurring in the family. Rare coexistence with oligophrenia. Clinical examinations, cytogenetic and HLA system
- Inpatient management of adolescent psychiatric patients. A single day study
- Intracranial plasma cell granuloma and homocystinuria
- Keratoconus in Albers-Schönberg disease
- Madness in the Old Norse society. Narratives and ideas
- Mental disorders as an indication for surgical treatment of drug-resistant temporal lobe epilepsy
- Microphthalmia, marked short stature, hearing loss, and developmental delay: extension of the phenotype of GOMBO syndrome?
- MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement
- Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes
- Mutations associated with Sjögren-Larsson syndrome
- Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)
- Neuroectodermal dysplasia in 2 Uzbek families
- Neuroleptics in mentally retarded children
- Neuropsychiatric disorders in newborn infants with very low birth weight (VLBW infants)--before and following introduction of modern perinatal medicine. 1. Overview of the problem, criteria for quality of survival, major CNS disorders (major handicap)
- Neuropsychiatric disorders in newborn infants with very low birth weight (VLBW infants)--before and following introduction of modern perinatal medicine. 2. Infantile cerebral palsy, epilepsy and mental handicap (oligophrenia)
- Neuropsychiatric disorders in very-low-birthweight newborn infants (VLBW-infants)--before and after the introduction of modern perinatal medicine. 3. Discussion of trends in quality of survival (CNS morbidity) and conclusions
- NLS-3 (Levophacetoperane or (<em>R,R</em>) Phacetoperane): A Reverse Ester of Methylphenidate: A Literature Review
- NLS-3 (Levophacetoperane or (R,R) Phacetoperane): A Reverse Ester of Methylphenidate: A Literature Review
- Oculo-dento-digital syndrome (Gorlin's syndrome): clinical and genetical report of a new family
- Oligophrenia as a disability diagnosis. Disability pensions in the period 1967-1992 in a group from Bergen born in 1940
- Ontogenesis of neurocognitive development of children and adolescents
- Pathological structure of blood vessels of cerebral cortex in Alzheimer's disease in comparison with various other types of mental retardation (oligophrenia, Down's syndrome)
- Percutaneous coronary angioplasty of unprotected left main stem: a case report
- Primary hypogonadism associated with neuropsychiatric disorders
- Progression of hepatic fibrosis observed by repeated liver biopsies in an adult case of COACH syndrome
- Pseudohypoparathyroidism--a case report
- Psychoses in children with oligophrenia
- Psychotic syndromes in patients with organic brain damage in the light of clinical analysis
- Rectal prolapse: etiopathogenetic and therapeutic problems in psychiatric patients
- Recurrent dysregulation of body temperature during antipsychotic pharmacotherapy
- Renal insufficiency is a component of COACH syndrome
- Report of a case: acromesomelic dysplasia: radiologic, clinical, and pathological study
- Richards-Rundle syndrome
- Robin-Silverman-Smith (fetal face) syndrome
- Schizophrenia in adolescence
- Screening of mentally retarded persons for "fragile" X-chromosome
- Sjogren-Larsson syndrome: A rare neurocutaneous disorder
- Sjögren-Larsson syndrome: report of a case in India
- Some Italian research on the phenomenon of filicide
- Status of problems with administration of hormonal contraceptives
- Structural and dynamic characteristics of patients with oligophrenia at a forensic-psychiatric clinic
- Successful combined liver and kidney transplant for COACH syndrome and 5-yr follow-up
- Sudden death of an 18-year-old man with homocystinuria and intracranial inflammatory pseudotumor (IPT)
- Sukhareva's (1930) 'Toward the problem of the structure and dynamics of children's constitutional psychopathies (Schizoid forms)': a translation with commentary
- Suspected Autosomal Recessive Polycystic Kidney Disease but Cerebellar Vermis Hypoplasia, Oligophrenia Ataxia, Coloboma, and Hepatic Fibrosis (COACH) Syndrome in Retrospect, A Delayed Diagnosis Aided by Genotyping and Reverse Phenotyping: A Case Report an
- Swallowing foreign bodies as an example of impulse control disorder in a patient with intellectual disabilities: a case report
- Syndrome forms of complicated oligophrenia (Rubinstein-Taybi and Noonan syndromes)
- Targeted phosphotyrosine profiling of glycoprotein VI signaling implicates oligophrenin-1 in platelet filopodia formation
- Tetra-X syndrome with epilepsy, mental retardation and multiple dysmorphias
- The De Barsy syndrome
- The dentomaxillofacial characteristics of the Prader-Labhart-Willi syndrome. A clinical case report
- The discovery of phenylketonuria
- The dynamics of oligophrenia from the forensic psychiatric aspect
- The evolution of the canons law code and the mental nature reasons of marital incapacity during the last 25 years
- The first Japanese case of COACH syndrome
- The indices of the thrombocyte serotonin system and of the nerve growth factor system in children with hereditary disorders of neuropsychic development
- The Marinescu-Sjögren syndrome
- The temporal correlations of the VEP of the visual and motor cortices during the perception and mental reproduction of an image in normal children and in those with intellectual disorders
- Thoracoscopic removal of dental prosthesis impacted in the upper thoracic esophagus
- Visual evoked potentials and functional asymmetry in children with with different degrees of intellectual retardation