Zobrazeno 1 - 7
of 7
pro vyhledávání: '"L M, Smit"'
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 145(17)
In children with head injuries the severity of the neurological symptoms should concord with the patient's history and signs of neurotrauma on examination. Discrepancies between the (hetero)anamnesis and physical examination on the one hand and neuro
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 144(4)
Three previously healthy children, two girls aged 2 and almost 5 years and a boy aged 20 months, developed a progressively stumbling gait within days. In two this occurred after a period of weeks during which they complained of, or seemed to have bac
Autor:
L M, Smit, E G, Hageman
Publikováno v:
Tijdschrift voor kindergeneeskunde. 57(3)
Two congenital anterior horn cell diseases may be responsible for neonatal muscular atrophy. The acute Werdnig-Hoffmann disease (SMA-I) has a progressive course, the anterior horn cell degeneration (AHCD) is non progressive in the postnatal period. I
Publikováno v:
Monographs in allergy. 25
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 132(11)
Autor:
F W, Bertelsmann, L M, Smit
Publikováno v:
Clinical neurology and neurosurgery. 87(2)
A 9-year-old girl suffering from progressive fluctuating dystonia is reported. Some problems of diagnosis are discussed. The differential diagnosis is described and a comparison is made with cases from the literature.
Publikováno v:
Clinical genetics, 34(2), 135-139. Wiley-Blackwell
A newborn is described in whom trisomy 12 mosaicism was detected prenatally at third trimester amniocentesis during the fourth pregnancy of a 34-year-old woman. After birth, trisomy 12 cells were found in placental tissue and in cultured urine sedime