Medline Abstracts, Arthrogryposis, 1989-96

Titles:

• Comparison of nicotinic receptor binding and biotransformation of coniine in the rat and chick
  
  
• Transient neonatal arthrogryposis: another case
  
  
• Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?
  
  
• Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor function
  
  
• Extending the spectrum of distal arthrogryposis
  
  
• Distal arthrogryposis type 1: clinical analysis of a large kindred
  
  
• A revised and extended classification of the distal arthrogryposis
  
  
• Pena-Shokeir phenotype associated with bilateral opercular polymicrogyria
  
  
• Hydranencephaly, cerebellar hypoplasia, and myopathy in chick embryos infected with aino virus
  
  
• Arthrogryposis associated with unsuccessful attempts at termination of pregnancy
  
  
• Incidence of maxillofacial involvement in arthrogryposis multiplex congenita
  
  
• Medial-approach open reduction of hip dislocation in amyoplasia-type arthrogryposis
  
  
• Distal femoral extension osteotomy for knee flexion contracture in patients with arthrogryposis
  
  
• Diagnosis and management of tendon disorders in cattle
  
  
• The role of the pediatrician in prescribing therapy services for children with motor disabilities
  
  
• Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings
  
  
• Arthrogryposis multiplex congenita and bilateral parietal polymicrogyria in association with the intrauterine death of a twin
  
  
• Arthrogryposis multiplex congenita, AD 1156
  
  
• Amyoplasia, the most common type of arthrogryposis: the potential for good outcome
  
  
• The myopathic variety of arthrogryposis multiplex congenita
  
  
• Helping to solve problems associated with spina bifida
  
  
• Pelvic kidney: a rare cause of obstetrical obstruction
  
  
• Lethal arthrogryposis multiplex congenital (fetal akinesia deformation sequence, FADS)
  
  
• Distal arthrogryposis type IIB: further clinical delineation and 54-year follow-up of an index case
  
  
• Prenatal findings in generalized amyoplasia
  
  
• Arthrogryposis, renal dysfunction and cholestasis syndrome: report of five patients from three Italian families
  
  
• A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3-q11.2
  
  
• Ultrasound diagnosis of the Pena Shokeir phenotype at 14 weeks of pregnancy
  
  
• Epilepsy in the Freeman Sheldon syndrome
  
  
• Epileptic seizures, arthrogryposis, and migrational brain disorders: a syndrome?
  
  
• Two sisters with Escobar syndrome
  
  
• Fetal hypokinesia syndrome in the monochorionic pair of a triplet pregnancy secondary to severe disruptive cerebral injury
  
  
• Familial scleroderma-like deformity of the fingers
  
  
• Neuroaxonal degeneration in sheep grazing Sorghum pastures
  
  
• Arthrogryposis multiplex congenita due to congenital myasthenic syndrome
  
  
• Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region
  
  
• Clubfoot deformity in Down's syndrome
  
  
• Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigen
  
  
• Periarticular fractures after manipulation for knee contractures in children
  
  
• Congenital idiopathic clubfoot deformities
  
  
• The familial syndrome of proliferative vasculopathy and hydranencephaly-hydrocephaly: immunocytochemical and ultrastructural evidence for endothelial proliferation
  
• Dominant distal arthrogryposis in a Maori family with marked variability of expression
  
  
• A cognitively normal boy with meningoencephalocele, arthrogryposis and hypoplastic thumbs
  
  
• Arthrogryposis multiplex congenita in an Arab kindred: update
  
  
• Recurrent congenital arthrogryposis leading to a diagnosis of myasthenia gravis in an initially asymptomatic mother
  
  
• Lethal congenital contracture syndrome (LCCS), a fetal anterior horn cell disease, is not linked to the SMA 5q locus
  
  
• Lethal arthrogryposis with anterior horn cell disease
  
  
• Lethal arthrogryposis in Finland--a clinico-pathological study of 83 cases during thirteen years
  
  
• Akabane virus
  
  
• The association of cortical dysplasia and anterior horn arthrogryposis: a case report
  
  
• A congenital abnormality of calves, suggestive of a new type of arthropod-borne virus infection
  
  :
• Epileptic seizures, arthrogryposis, and migrational brain disorders: a syndrome?
  
  
• Arthrogryposis multiplex congenita, renal dysfunction, and cholestasis syndrome
  
  
• Foot deformities in arthrogryposis multiplex congenita
  
  
• A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9
  
  
• Lethal congenital contracture syndrome: further delineation and genetic aspects
  
  
• Familial infantile myasthenia: a neuromuscular cause of respiratory failure
  
  
• Early surgical treatment for congenital vertical talus
  
  
• Multiple pterygium syndrome (Escobar syndrome)--a case report
  
  
• An approach to ventilator-dependent neonates with arthrogryposis
  
  
• Arthrogryposis multiplex congenita: a report of two cases
  
  
• Congenital myopathy with fiber type disproportion: a family with a chromosomal translocation t(10;17) may indicate candidate gene regions
  
  
• Middle ear deformity in arthrogryposis multiplex congenita
  
  
• Effect of coniine on the developing chick embryo
  
  
• Fatal arthrogryposis with respiratory insufficiency: a possible case of muscle phosphorylase b-kinase deficiency
  
  
• Talectomy for osteoporotic and neuropathic feet. 7 cases followed for 2-3 years
  
  
• Ambulatory monitoring of the sudden death of an adolescent with hypertrophic cardiomyopathy
  
  
• Lethal congenital muscular dystrophy with arthrogryposis multiplex congenita: three new cases and review of the literature
  
  
• Congenital muscular dystrophy with distinct CNS involvement
  
  
• Duane's retraction syndrome and arthrogryposis multiplex congenita
  
  
• Liver histology in the arthrogryposis multiplex congenita, renal dysfunction, and cholestasis (ARC) syndrome: report of three new cases and review
  
  
• Dominant congenital benign spinal muscular atrophy
  
  
• Investigations on the occurrence of hereditary diseases in the Danish cattle population 1989- 199
  
  
• An additional case of pachygyria, joint contractures and facial abnormalities
  
  
• Neurogenic arthrogryposis multiplex congenita: clinical and MRI findings
  
  
• Arthrogryposis multiplex in a newborn of a myasthenic mother--case report and literature
  
  
• A congenital variant of glycogenosis type IV
  
  
• Soft-tissue expander failure in severe equinovarus foot deformity
  
  
• The diagnosis and orthopaedic treatment of childhood spinal muscular atrophy, peripheral neuropathy, Friedreich ataxia, and arthrogryposis
  
  
• Newly recognized autosomal recessive MCA/MR/overgrowth syndrome
  
  
• Joint contractures, hyperkeratosis, and severe hypoplasia of the posterior columns: a new recessive syndrome
  
  
• Familial bilateral antecubital pterygia with severe renal involvement in nail-patella syndrome
  
  
• Arthrogryposis multiplex congenita: report of a case of amyoplasia
  
  
• Distal arthrogryposis with autosomal dominant inheritance and reduced penetrance in females: the Gordon syndrome
  
  
• Lethal multiple pterygium syndrome: report of a case with neurological anomalies
  
  
• Alpers progressive infantile neuronal poliodystrophy: an acute neonatal form with findings of the fetal akinesia syndrome
  
  
• Multiple pterygium syndrome with body asymmetry
  
  
• A novel nonsense mutation, W846XI (amber termination), in exon 14a of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
  
  
• Arthrogryposis multiplex congenita with renal and hepatic abnormalities
  
  
• Hydranencephaly in newborn calves in Zambia
  
  
• Evaluation of developmental toxicity of coniine to rats and rabbits
  
  
• Antepartum diagnosis of arthrogryposis associated with trisomy 18
  
  
• Early corrective surgery of the wrist and elbow in arthrogryposis multiplex congenita
  
  
• Early prenatal sonographic diagnosis of neuropathic arthrogryposis multiplex congenita with osseous heterotopia
  
  
• Muscle ultrasonography in arthrogryposis. Comparison with clinical, neuromyographic and histologic findings in 41 cases
  
  
• Use of tissue expansion in clubfoot surgery
  
• Congenital cervical spinal muscular atrophy: a non-familial, non progressive condition of the upper limbs
  
  
• Congenital defects of the bovine musculoskeletal system and joints
  
  
• Quinolizidine and piperidine alkaloid teratogens from poisonous plants and their mechanism of action in animals
  
  
• An outbreak of Akabane virus-induced abnormalities in calves after agistment in an endemic region
  
  
• Congenital dislocation of the knee. Its pathologic features and treatment
  
  
• Restrictive dermopathy: a lethal congenital skin disorder
  
  
• Arthrogryposis multiplex congenita with posterior column degeneration and peripheral neuropathy: a case report
  
  
• Prenatal diagnosis of distal arthrogryposis type I by ultrasonography
  
  
• Multiple congenital contractures (arthrogryposis) in association with Peters' anomaly and chorioretinal colobomata
  
  
• Lethal multiple pterygium syndrome
  
  
• Distal arthrogryposis, mental retardation, whistling face, and Pierre Robin sequence: another case
  
  
• Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis
  
  
• A large inbred Palestinian family with two forms of muscular dystrophy
  
  
• New hereditary malformation syndrome of unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defects
  
  
• Restrictive dermopathy: a disorder of fibroblasts
  
  
• Predictive value of electromyography in diagnosis and prognosis of the hypotonic infant
  
  
• Clinical variation within sibships in Fukuyama-type congenital muscular dystrophy
  
  
• Congenital caudal spinal atrophy: a case report
  
  
• Ehlers-Danlos syndrome with soft-tissue contractures
  
  
• The use of vacuum-molded polyvinyl acetate-polyethylene copolymer (PVAC.PE) for a handicapped patient
  
  
• Skin expansion as preparation for an opening wedge osteotomy of the mid-foot in arthrogryposis
  
  
• Clinical features for prediction of survival in neonatal muscle disease
  
  
• Goniodysgenesis of the eye with arthrogryposis multiplex congenita
  
  
• Transportation resources for pediatric orthopaedic clients
  
  
• Congenital hypomyelination neuropathy with arthrogryposis multiplex congenita
  
  
• Restrictive dermopathy, a lethal form of arthrogryposis multiplex with skin and bone dysplasias: three new cases and review of the literature

[ more > ]