Zobrazeno 1 - 10
of 97
pro vyhledávání: '"S Jagell"'
Publikováno v:
Acta Ophthalmologica. 58:321-330
All Swedish cases with the Sjögren-Larsson syndrome (SLS) i.e. 35 patients were studied. Glistening dots of unknown nature were seen round the foveola. These foveal and parafoveal changes seem to be a cardinal sign of SLS together with congenital ic
Publikováno v:
Lakartidningen. 92(28-29)
Publikováno v:
Neuroradiology. 21:101-105
Cranial computed tomography was performed on five patients with the Sjögren-Larsson syndrome (SLS). No specific morphological abnormalities were found, nor was there any indication of a reduction of brain mass. This result is in keeping with the fin
Autor:
P.‐Å. Hofer, S. Jagell
Publikováno v:
Journal of Cutaneous Pathology. 9:360-376
Thirty-six Swedish patients with the recessively inherited Sjögren-Larsson syndrome (SLS) were examined by histopathologic and, in some cases, morphometric techniques. Skin biopsy specimens were taken on the volar side of the right forearm below the
Publikováno v:
ASDC journal of dentistry for children. 56(1)
Neuromotor handicaps and mental retardation have been associated with various types of dental malocclusions and oral dysfunction. In this study the specific role of mental status on oral functions was examined. For this, oral function capacity was co
Publikováno v:
Swedish dental journal. 9(1)
Dental health of 103 children with severe mental retardation living in the north of Sweden, has been surveyed and compared with that of a control group of healthy children of normal intelligence. Data has been related to medical diagnosis, medication
Publikováno v:
Human heredity. 34(4)
A mixture of clinical signs seen in diastrophic dysplasia as well as in trisomy 18 was found in two siblings with an E trisomy mosaicism. The E trisomy mosaicism was present in blood and skin during the first years of life, but disappeared later on.
Publikováno v:
Swedish dental journal. 11(3)
The purpose of this work was to study the morphological characteristics of dental occlusion in groups of physically and/or mentally handicapped children, taking into consideration the need of a detailed classification of medical diagnosis and degree
Autor:
L. Iselius, S. Jagell
Publikováno v:
Clinical genetics. 35(4)
The distribution of carriers of the gene for Sjogren-Larsson syndrome in Sweden suggests a center of dispersion in the county of Vasterbotten in Northern Sweden. The origin of the spread of the gene can be traced back at least 700 years.
Autor:
S, Jagell, P A, Hofer
Publikováno v:
Acta dermato-venereologica. 62(5)
Replicas of the skin below the cubital fossa were made in 29 SLS patients with an age range of 8 days to 69 years. The skin surface patterns differed from those in healthy controls. The papillomatosis observed in most SLS replicas seemed to appear du