|1.||Hübner, Christoph: 2 articles (05/2013 - 08/2006)|
|2.||Steinlein, Ortrud K: 2 articles (01/2008 - 05/2007)|
|3.||Lochmüller, Hanns: 2 articles (08/2006 - 11/2004)|
|4.||Pavone, P: 2 articles (12/2001 - 12/2000)|
|5.||Parano, E: 2 articles (12/2001 - 12/2000)|
|6.||Newsom-Davis, J: 2 articles (07/2001 - 05/2000)|
|7.||Vincent, A: 2 articles (07/2001 - 05/2000)|
|8.||Omran, Ahmed A: 1 article (11/2015)|
|9.||El-Sherbini, Mostafa H: 1 article (11/2015)|
|10.||Chotigavanichaya, Chatupon: 1 article (09/2015)|
06/01/2008 - "The inclusion criteria for this study were as follows: patients diagnosed with arthrogryposis multiplex congenita group 1, a knee extension contracture present from birth, follow-up from birth or early childhood, at least yearly physical examinations, and a knee ultrasonography or magnetic resonance imaging study performed. "
01/01/1990 - "Open reduction will be indicated in three circumstances: failure to correct the soft tissue contracture; failure of the hip to reduce concentrically following a "Trial of Closed Reduction"; and when closed reduction is contra-indicated in a child over two and a half years or with an associated condition such as Arthrogryposis Multiplex Congenita."
06/04/2015 - "Arthrogryposis multiplex congenita is defined by the presence of contractures across two or more major joints and results from reduced or absent fetal movement. "
01/01/2015 - "Arthrogryposis Multiplex Congenita: Multiple Congenital Joint Contractures."
10/01/2014 - "Both pregnancies presented with clinical features of arthrogryposis multiplex congenita/fetal akinesia syndrome (AMC/FAS), including clenched fists and multiple joint contractures on repeat prenatal ultrasound examinations. "
|2.||Clubfoot (Talipes Equinovarus)
01/01/1997 - "We believe that it is advisable to wait 1 month for spontaneous reduction of CDK in cases not associated with clubfoot, arthrogryposis multiplex congenita, and Larsen's syndrome."
09/01/2015 - "Results of Primary Talectomy for Clubfoot in Infants and Toddlers with Arthrogryposis Multiplex Congenita."
11/01/1984 - "Two had talipes equinovarus, one had congenital hip subluxation, and the youngest had arthrogryposis multiplex congenita. "
09/15/1962 - "Experimental clubfoot and arthrogryposis multiplex congenita."
09/01/2015 - "Arthrogryposis multiplex congenita patients with rigid equinovarus deformity treated with talectomy initially were retrospectively reviewed. "
|4.||Congenital Abnormalities (Deformity)
08/22/2004 - "To study the methods and effects of Ilizarov distraction technique in treating the flexion deformity of the knee of arthrogryposis multiplex congenita. "
09/01/2013 - "The results in arthrogryposis multiplex congenita were noteworthy for the absence of extensor weakness, postoperative deformity, or recurrence. "
05/01/2005 - "Eight patients with arthrogryposis multiplex congenita (amyoplasia type) (11 knees) with knee hyperextension deformity underwent quadricepsplasty and were analyzed during an average follow-up period of 11 years and 2 months. "
04/01/1999 - "Plasma from human mothers of fetuses with severe arthrogryposis multiplex congenita causes deformities in mice."
09/01/1994 - "Middle ear deformity in arthrogryposis multiplex congenita."
|5.||Muscular Diseases (Myopathy)
02/01/2015 - "Clinical features in affected infants ranged from a mild predominantly facial and bulbar myopathy to arthrogryposis multiplex congenita. "
07/01/1998 - "This congenital nonprogressive myopathy is not as benign as previously thought and may be an etiology of the lethal form of arthrogryposis multiplex congenita. "
01/01/1991 - "A hydropic fetus with translucent ribs, arthrogryposis multiplex congenita and congenital myopathy: etiological heterogeneity of A.M.C., Toriello-Bauserman type?"
01/01/1979 - "A review of 15 cases in the literature revealed this type of myopathy as a distinctive entity to be classified as a myopathic arthrogryposis multiplex congenita, rather than in the group of muscular dystrophies."
01/01/1988 - "Thirteen cases of arthrogryposis multiplex congenita without evidence of spinal muscular atrophy, congenital muscular dystrophy, or structural myopathy were reviewed. "
|1.||Congenital Talipes Equinovarus
|2.||Multiple pterygium syndrome
|3.||mental subnormality pyorrhea epilepsy Alopecia
|4.||Congenital contractural arachnodactyly
|5.||Arthrogryposis renal dysfunction cholestasis syndrome
|8.||Ion Channels (Ion Channel)
|10.||gamma-Glutamyltransferase (gamma-Glutamyl Transpeptidase)
|2.||Positive-Pressure Respiration (PEEP)