Zobrazeno 1 - 10
of 66
pro vyhledávání: '"K, Taudorf"'
Autor:
Karen Brøndum-Nielsen, H Simonsen, Susanne Kjaergaard, B Hamborg-Petersen, A E Jønch, Maria Kirchhoff, L Roos, K Taudorf
Publikováno v:
Journal of Medical Genetics. 46:703-710
Background: The use of array CGH analyses for investigation of mentally retarded children has led to the identification of a growing number of new microdeletion and microduplication syndromes, some of which have become clinically well characterised,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7edb81a8b4883c48f879b49ae2dd396
https://doi.org/10.1136/jmg.2008.065094
https://doi.org/10.1136/jmg.2008.065094
Publikováno v:
Acta Paediatrica. 89:58-63
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a34ef1458dacb03c05e3b06d6c04e1c
https://doi.org/10.1111/j.1651-2227.2000.tb01188.x
https://doi.org/10.1111/j.1651-2227.2000.tb01188.x
Autor:
K, Taudorf
Publikováno v:
Ugeskrift for laeger. 163(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f606ab4aa6ab67dbcc8604d2ffe6ec3f
https://pubmed.ncbi.nlm.nih.gov/11347463
https://pubmed.ncbi.nlm.nih.gov/11347463
Autor:
P V, Uldall, F J, Hansen, B, Beck, J M, Buchholt, F U, Knudsen, L B, Lassen, K, Lee, K, Taudorf
Publikováno v:
Ugeskrift for laeger. 160(39)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0ddbd7259aa9d241100c092a166ec71
https://pubmed.ncbi.nlm.nih.gov/9771069
https://pubmed.ncbi.nlm.nih.gov/9771069
Publikováno v:
Ugeskrift for laeger. 157(38)
The clinical, neuroradiological and biochemical findings in two siblings with molybdenum cofactor deficiency are presented. A search for this deficiency is advocated in each case of unexplained refractory neonatal convulsions. Early diagnosis is prom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2dd16088852f8771b38a5d3509385570
https://pubmed.ncbi.nlm.nih.gov/7483042
https://pubmed.ncbi.nlm.nih.gov/7483042
Autor:
H R, Lie, J, Lagergren, F, Rasmussen, B, Lagerkvist, J, Hagelsteen, M C, Borjeson, M, Muttilainen, F K, Taudorf
Publikováno v:
European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dccec9c03d03cc7934b6093ddd33c3b5
https://pubmed.ncbi.nlm.nih.gov/1807386
https://pubmed.ncbi.nlm.nih.gov/1807386
Publikováno v:
European Journal of Paediatric Neurology. 11:122
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f43cb53e9a5cc52523981ae5827eb5b9
https://doi.org/10.1016/s1090-3798(08)70722-0
https://doi.org/10.1016/s1090-3798(08)70722-0
Publikováno v:
Neuroradiology. 23(5)
Eighty-three children with spastic cerebral palsy (CP) were examined with cranial CT. In 56 cases the CT findings were abnormal. The most frequent abnormality was atrophy, present in 44 patients. The frequency of pathologic CT increased with severity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d2f89b261e63a8489f914da6e2e70df
https://pubmed.ncbi.nlm.nih.gov/7121822
https://pubmed.ncbi.nlm.nih.gov/7121822
Publikováno v:
Acta chirurgica Scandinavica. 144(7-8)
Three cases of Klippel--Trenaunay--Weber's syndrome are presented. The syndrome is characterized by cutaneous hemangioma, hypertrophy of an extremity and varicose veins. It is combined with angiodysplasias, either in the form of aplasia/hypoplasia of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::adb056464fe8c21a526fd6f72b2342fe
https://pubmed.ncbi.nlm.nih.gov/218412
https://pubmed.ncbi.nlm.nih.gov/218412
Autor:
K, Sørensen, J, Nielsen, P, Busch, B, Hamborg-Petersen, E, Hansen, L B, Lassen, K, Nielsen, J P, Poulsen, K, Rossen, S K, Schaap, K, Taudorf, T, Thelle, S, Vestermark, C, Vrang
Publikováno v:
Ugeskrift for laeger. 141(14)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73b039420d1a649689afbe7655889d42
https://pubmed.ncbi.nlm.nih.gov/425192
https://pubmed.ncbi.nlm.nih.gov/425192