Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Huijmans, J."'
Autor:
Kornelisse, R. F., Hoekman, K., Visser, J. J., Hop, W. C. J., Huijmans, J. G. M., van der Straaten, P. J. C., van der Heijden, A. J., Sukhai, R. N., Neijens, H. J., de Groot, R.
Publikováno v:
The Journal of Infectious Diseases, 1996 Jul 01. 174(1), 120-126.
Externí odkaz:
https://www.jstor.org/stable/30126227
Autor:
T. Rabenstein, Ch. Ell, Liebwin Gossner, Manfred Stolte, Hendrik Manner, Huijmans J, Oliver Pech, M Vieth, Andrea May, E. Günter
Publikováno v:
Endoscopy. 40:899-904
Background and study aims Gastric cancer diagnosed from routine gastric biopsies without any evidence of a visible lesion and negative repeated biopsies is an infrequent but serious clinical problem for which gastrectomy has usually been recommended,
Autor:
Frints, S.g.m., Arens, Y., Bakker, J., Huijmans, J., Stevens, S., Engelen, J., Blok, R., Nijhuis, J., Willekes, C., Ten Haaft, A., Henskens, Y., Cleven, A., Baldewijns, M., Lissens, Willy, De Die-Smulders, C.e.m.
no abstract available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::87f8e843b8d0fb0cec1868d4ebde9043
https://biblio.vub.ac.be/vubir/recurrent-progressive-nonimmune-hydrops-foetalis-better-think-of-mucopolysaccharidoses-type-viibetaglucuronidase-deficiencygusb-gene-defect(67606b7b-4b43-4526-b9e2-818570de648b).html
https://biblio.vub.ac.be/vubir/recurrent-progressive-nonimmune-hydrops-foetalis-better-think-of-mucopolysaccharidoses-type-viibetaglucuronidase-deficiencygusb-gene-defect(67606b7b-4b43-4526-b9e2-818570de648b).html
Autor:
Williams, M., Huijmans, J. G. M., Duran, M., de Klerk, J. B. C., van Maldegem, B. T., Poll-The, B. T.
Publikováno v:
Nederlands tijdschrift voor geneeskunde, 151(21), 1191-1196. Bohn Stafleu van Loghum
The data from 5 clinics concerning 8 infants, who had developed severe lactic acidosis and hyperglutamic acidaemia were reviewed. Blood-lactate levels were up to 15 mmol/l (reference level: < 2) and plasma-glutamate levels up to 1632 pmol/l (referenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::51960bcde9d4ab84865a13b956917cd0
https://pure.amc.nl/en/publications/lactaatacidose-en-glutamaatophoping-in-het-bloed-van-neonaten-na-behandeling-met-calciumlevulaat-wegens-hypocalciemie(aa726943-3158-4615-885d-5032bbc3da54).html
https://pure.amc.nl/en/publications/lactaatacidose-en-glutamaatophoping-in-het-bloed-van-neonaten-na-behandeling-met-calciumlevulaat-wegens-hypocalciemie(aa726943-3158-4615-885d-5032bbc3da54).html
Publikováno v:
Nederlands Tijdschrift voor Geneeskunde, 149, 2789-2794. Bohn Stafleu van Loghum
Nederlands tijdschrift voor geneeskunde, 149(50), 2789-2794. Bohn Stafleu van Loghum
Nederlands tijdschrift voor geneeskunde, 150(8). Bohn Stafleu van Loghum
Nederlands tijdschrift voor geneeskunde, 149(50), 2789-2794. Bohn Stafleu van Loghum
Nederlands tijdschrift voor geneeskunde, 150(8). Bohn Stafleu van Loghum
Vitamin B12 (cobalamin) deficiency is a common disorder with potential irreversible haematological and neurological consequences. Currently used diagnostic tests such as the evaluation of serum vitamin B12 and the Schilling test are insufficient, e.g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b359693bba09a77281515dc90ea1e636
https://pure.eur.nl/en/publications/517076c3-06c8-4f12-914a-eaecf0ae5c9e
https://pure.eur.nl/en/publications/517076c3-06c8-4f12-914a-eaecf0ae5c9e
Autor:
Mancini, G. M.S., Catsman-Berrevoets, C. E., De Coo, I. F.M., Aarsen, F. K., Kamphoven, J. H.J., Huijmans, J. G., Duran, M., Van Der Knaap, M. S., Jakobs, C., Salomons, G. S.
Publikováno v:
American journal of medical genetics. Part A, 132A(3), 288-295. Wiley-Liss Inc.
Mancini, G M S, Catsman-Berrevoets, C E, De Coo, I F M, Aarsen, F K, Kamphoven, J H J, Huijmans, J G, Duran, M, Van Der Knaap, M S, Jakobs, C & Salomons, G S 2005, ' Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families ', American Journal of Medical Genetics, vol. 132 A, no. 3, pp. 288-295 . https://doi.org/10.1002/ajmg.a.30473
American Journal of Medical Genetics, 132 A(3), 288-295. Wiley-Liss Inc.
Mancini, G M S, Catsman-Berrevoets, C E, De Coo, I F M, Aarsen, F K, Kamphoven, J H J, Huijmans, J G, Duran, M, Van Der Knaap, M S, Jakobs, C & Salomons, G S 2005, ' Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families ', American Journal of Medical Genetics, vol. 132 A, no. 3, pp. 288-295 . https://doi.org/10.1002/ajmg.a.30473
American Journal of Medical Genetics, 132 A(3), 288-295. Wiley-Liss Inc.
Four Dutch male patients, two brothers from unrelated families were referred for investigation of psychomotor and severe language/speech delay. All four patients showed growth deficiency over the years. Facial features and poor body habitus were quit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6600cf164d55e4747aa1ed9e262bb63f
https://pure.amc.nl/en/publications/two-novel-mutations-in-slc6a8-cause-creatine-transporter-defect-and-distinctive-xlinked-mental-retardation-in-two-unrelated-dutch-families(d5738848-1a0f-4309-aff7-9ac153a56044).html
https://pure.amc.nl/en/publications/two-novel-mutations-in-slc6a8-cause-creatine-transporter-defect-and-distinctive-xlinked-mental-retardation-in-two-unrelated-dutch-families(d5738848-1a0f-4309-aff7-9ac153a56044).html
Autor:
Jacek Zaremba, Kleijer, W. J., Huijmans, J. G. M., Poorthuis, B., Fidzianska, E., Glogowska, I.
Publikováno v:
Journal of medical genetics, 29(7). BMJ Publishing Group
Scopus-Elsevier
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d0a9e8dd2fe7937e4fc7da55fe8be201
https://pure.amc.nl/en/publications/chromosomes-14-and-21-as-possible-candidates-for-mapping-the-gene-for-sanfilippo-disease-type-iiic(e62d8581-83bd-4704-8468-a7813f6a8d30).html
https://pure.amc.nl/en/publications/chromosomes-14-and-21-as-possible-candidates-for-mapping-the-gene-for-sanfilippo-disease-type-iiic(e62d8581-83bd-4704-8468-a7813f6a8d30).html
Autor:
He, Wang, Voznyi, Ya. V., Huijmans, J. G. M., Geilen, G. C., Karpova, E. A., Dudukina, T. V., Zaremba, J., van Diggelen, O. P., Kleijer, W. J., He, W, Voznyi YaV, Huijmans, J G
Publikováno v:
Prenatal Diagnosis; Jan1994, Vol. 14 Issue 1, p17-22, 6p
Autor:
Wladimiroff, J. W., Niermeijer, M. F., Van Der Harten, J. J., Stewart, P. A., Versteegh, F. G. A., Blom, W., Huijmans, J. G. M., Versteegh, F G, Huijmans, J G
Publikováno v:
Prenatal Diagnosis; Jan1985, Vol. 5 Issue 1, p47-52, 6p
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.