Zobrazeno 1 - 10
of 907
pro vyhledávání: '"B, Hagberg"'
Autor:
G. Lockwood Estrin, V. Kyriakopoulou, A. Makropoulos, G. Ball, L. Kuhendran, A. Chew, B. Hagberg, M. Martinez-Biarge, J. Allsop, M. Fox, S.J. Counsell, M.A. Rutherford
Publikováno v:
NeuroImage: Clinical, Vol 11, Iss C, Pp 139-148 (2016)
Ventriculomegaly (VM) is the most common central nervous system abnormality diagnosed antenatally, and is associated with developmental delay in childhood. We tested the hypothesis that antenatally diagnosed isolated VM represents a biological marker
Externí odkaz:
https://doaj.org/article/9c0319375aa84bcebd8c0194a50a4d1e
Publikováno v:
Acta Societatis Botanicorum Poloniae, Vol 56, Iss 2, Pp 209-214 (2014)
The embryo sac haustorium found in Dryas octopetala L. from the Tatra Mts is the first record of its occurrence in Rosaceae. At the eight-nucleate stage of the embryo sac, the antipodal end of the central cell began to grow into a narrow caecum fille
Publikováno v:
Developmental Medicine & Child Neurology. 27:249-252
Autor:
I, Krägeloh-Mann, G, Hagberg, C, Meisner, B, Schelp, G, Haas, K E, Eeg-Olofsson, H K, Selbmann, B, Hagberg, R, Michaelis
Publikováno v:
Developmental Medicine & Child Neurology. 36:473-483
Epidemiological data of a collaborative study on children with bilateral spastic cerebral palsy (BSCP) between south-west Germany and western Sweden are reported. The study period covered the birth years 1975 to 1986. Overall, the rate of BSCP increa
Publikováno v:
Acta Paediatrica. 90:271-277
UNLABELLED This 8th Swedish population-based cerebral palsy (CP) report comprises 241 children born 1991-94. The live birth prevalence was 2.12 per 1000. Excluding 7 postnatally-derived cases, the gestational age-specific prevalences were 86 for extr
Publikováno v:
Acta Paediatrica. 91:946-951
Publikováno v:
Acta Paediatrica. 90:34-39
UNLABELLED In a representative series of 53 females with Rett syndrome (RS), aged 5-55 y, a history of epilepsy was present in 50 (94%), 45 of whom had 5-y active epilepsy. Compared with severe mental retardation in general, the median age of seizure
Autor:
B. Hagberg
Publikováno v:
Journal of Child Neurology. 20:722-727
Long-term clinical profiles of female patients with classic Rett syndrome are presented and exemplified by three cases, as experienced over four decades. Emphasized is the frequently surprisingly well-preserved eye contact and primitive memory, in co
Autor:
K. D. Bachmann, H. Berger, J. Bierich, D. Boda, H.-J. Bremer, J. Brodehl, G. R. Burgio, K. Fischer, E. Gladtke, B. Hadorn, B. Hagberg, N. Hallman, H. G. Hansen, H. Harbauer, G.-A. von Harnack, W. C. Hecker, H. Helge, W. H. Hitzig, E. Huth, E. Kleihauer, W. Künzer, M. A. Lassrich, B. Leiber, B. Lindquist, W. Marget, J. Oehme, H. Olbing, R. A. Pfeiffer, A. Prader, K. Riegel, E. Rossi, K. Schärer, E. Schmidt, F.-J. Schulte, H. Spiess, J. Spranger, G. Stalder, U. Stephan, J. Stoermer, J. Ströder, W. Teller, R. Zetterström, E. Zweymüller
Publikováno v:
European Journal of Paediatric Neurology. 7:417-421
A 25-year-old MECP2-mutated female with odd developmental and dyspraxic/ataxic features, followed up through two decades, is reported. She does not fit either the classical Rett syndrome or the criteria required for any Rett variant phenotypes so far