نتایج جستجو برای: von recklinghausen
تعداد نتایج: 96693 فیلتر نتایج به سال:
Three chromosome 19 markers known to be linked to myotonic dystrophy have been studied in nine families with peripheral neurofibromatosis (Von Recklinghausen's disease). Clear evidence against linkage has been found for all three markers, excluding the peripheral neurofibromatosis gene from the myotonic dystrophy region of chromosome 19. Previous reports of co-inheritance of the two disorders i...
Neurofibromatosis type 1 (NF-1) is one of the most common autosomal dominant disorders affecting humans. Patients with NF-1 may present with characteristic orthopaedic manifestations such as scoliosis, congenital pseudoarthrosis and limb hyperttrophy. Dislocation of the hip associated with NF-1 is a rare occurrence. There is a relative paucity of reported cases of pathological hip dislocation i...
From the Division of Neurosurgery (Drs. El-Watidy, A. Jamjoom, Z. Jamjoom), King Khalid University Hospital, Riyadh and Department of Neurosurgery (Or. Selen), Northern Area Armed Forces Hospital, Hafer AI-Batin. Address reprint requests and correspondence to Or. A. Jamjoom: Consultant Neurosurgeon, Division of Neurosurgery, King Khalid University Hospital, p.a. Box 2925, Riyadh 11461, Saudi Ar...
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