• 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