Avenues: A National Support Group for Arthrogryposis Multiplex Congenita | Medline Abstracts, Arthrogryposis, 1997-1998

Severe mental retardation-distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25-->qter deletion
Congenital Rapidly Fatal Form of Nemaline Myopathy with Fetal Hydrops and Arthrogryposis. a case report and review
Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24
Large-scale deletions in a Chinese infant associated with a variant form of Werdnig-Hoffmann disease
Improved oxygenation following adenosine infusion in persistent pulmonary hypertension of the newborn
Marden-Walker syndrome versus isolated distal arthrogryposis: evidence that both conditions may be variable manifestations of the same mutated gene
Newly described form of X-linked arthrogryposis maps to the long arm of the human X chromosome
Surgical management of hip dislocation in children with arthrogryposis multiplex congenita
Distal arthrogryposis, ectodermal dysplasia and dilated cardiomyopathy—a new syndrome?
Teratogenic and fetotoxic effects of two piperidine alkaloid-containing lupines (L. formosus and L. arbustus) in cows
An animal model of maternal antibody-mediated arthrogryposis multiplex congenita (AMC)
Antibodies affecting ion channel function in acquired neuromyotonia, in seropositive and seronegative myasthenia gravis, and in antibody-mediated arthrogryposis multiplex congenita
Anaesthesia in handicapped children
Disorders of the upper extremity in children
Congenital anomalies and vascular birthmarks of the lower extremities
Outpatient care of young invalids with locomotor defects
Total joint replacement in multiplex congenita contractures: a case report
Congenital abnormalities in Brazilian children associated with misoprostol misuse in first trimester of pregnancy
Modified Toupet wrap for gastroesophageal reflux in childhood
A severe case of Moebius syndrome with calcification on the fourth ventricular floor
Muscle and tendon size relationships in a paralyzed chick embryo model of clubfoot
Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness
Management of clubfoot deformity in amyoplasia
Microlissencephaly
The sequence of fetal akinesia/hypokinesia, Pena-Shokeir syndrome, multiple congenital arthrogryposis and/or short umbilical cord: conceptual delimitation
Cases of congenital dislocation of the knee (CDK) not associated with clubfoot, arthrogryposis multiplex congenita, and Larsen's syndrome can be treated conservatively
Congenital clasped thumb
Clinical analysis of a variant of Freeman-Sheldon syndrome (DA2B)
Prenatal growth retardation, pelvic hypoplasia, and arthrogrypotic changes of lower limbs: a distinct autosomal-recessive disorder
Bruck syndrome: a rare combination of bone fragility and multiple congenital joint contractures
Maternal serum screening abnormality in a fetus associated with arthrogryposis multiplex congenita and amyoplasia
Proteus syndrome and distal arthrogryposis
Amish miracle baby
Infantile phosphofructokinase deficiency with arthrogryposis: clinical benefit of a ketogenic diet
The pediatric high-risk patient in orthopedic surgery
Ragged-red fibers and complex I deficiency in a neonate with arthrogryposis congenita
Fetal akinesia deformation sequence in a highly developed acardius twin
Osteogenesis imperfecta with arthrogryposis multiplex congenita (Bruck syndrome)--evidence for possible autosomal recessive inheritance
Successful separation of thoraco-omphalopagus and ischiopagus tetrapus twins in Korea
Intraoperative convulsions in a child with arthrogryposis
A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter
Cerebral defects and nephrogenic diabetes insipidus with the ARC syndrome: additional findings or a new syndrome (ARCC-NDI)?
Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patients
Arthrogryposis due to infantile neuronal degeneration associated with deletion of the SMNT gene
Microcephaly with agenesis of corticospinal tracts and arthrogryposis, hypospadias, single umbilical artery, hypertelorism, and renal and adrenal hypoplasia--previously undescribed syndrome
Arthrogryposis multiplex congenita, craniofacial, and ophthalmological abnormalities and normal intelligence: a new syndrome?
Earliest evidence for arthrogryposis multiplex congenita or Larsen syndrome?
Arthrogrypotic joint contracture at the knee and the foot: correction with a circular frame
Management of knee deformity in classical arthrogryposis multiplex congenita (amyoplasia congenita)
Principles of treatment of the upper extremity in arthrogryposis multiplex congenita type I
Multiple congenital contractures
Arthrogryposis multiplex congenita: perinatal and electromyographic findings, disability, and psychosocial outcome
Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach, and general aspects


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