Tønnesen TI - Search Results

1

Clinical and Angiographic Outcome of Coronary Surgery with and without Cardiopulmonary Bypass: A Prospective Randomized Trial.

Lingaas PS, Hol PK, Lundblad R, Rein KA, Tønnesen TI, Svennevig JL, Hauge SN, Vatne K, Fosse E. Lingaas PS, et al. Among authors: tonnesen ti. Heart Surg Forum. 2004 Jan 1;7(1):37-41. Heart Surg Forum. 2004. PMID: 14980848

2

Clinical and radiologic outcome of off-pump coronary surgery at 12 months follow-up: a prospective randomized trial.

Lingaas PS, Hol PK, Lundblad R, Rein KA, Mathisen L, Smith HJ, Andersen R, Thaulow E, Tønnesen TI, Svennevig JL, Hauge SN, Fredriksen PM, Andersen M, Fosse E. Lingaas PS, et al. Among authors: tonnesen ti. Ann Thorac Surg. 2006 Jun;81(6):2089-95. doi: 10.1016/j.athoracsur.2005.12.003. Ann Thorac Surg. 2006. PMID: 16731135 Clinical Trial.

3

Mental retardation in a patient with Maroteaux-Lamy.

Vestermark S, Tønnesen T, Andersen MS, Güttler F. Vestermark S, et al. Clin Genet. 1987 Feb;31(2):114-7. doi: 10.1111/j.1399-0004.1987.tb02779.x. Clin Genet. 1987. PMID: 3103957

4

Normal MPS excretion, but dermatan sulphaturia, combined with a mild Maroteaux-Lamy phenotype.

Tønnesen T, Gregersen HN, Güttler F. Tønnesen T, et al. J Med Genet. 1991 Jul;28(7):499-501. doi: 10.1136/jmg.28.7.499. J Med Genet. 1991. PMID: 1832719 Free PMC article.

5

Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate.

Tønnesen T, Lykkelund C, Güttler F. Tønnesen T, et al. Hum Genet. 1982;60(2):167-71. doi: 10.1007/BF00569706. Hum Genet. 1982. PMID: 6210620

6

Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome.

Tønnesen T, Güttler F, Lykkelund C. Tønnesen T, et al. Hum Genet. 1983;64(4):371-5. doi: 10.1007/BF00292369. Hum Genet. 1983. PMID: 6225723

7

[Mucopolysaccharidoses].

Gerdes AM, Tønnesen T, Lykkelund C, Hobolth N, Güttler F. Gerdes AM, et al. Ugeskr Laeger. 1987 May 25;149(22):1439-43. Ugeskr Laeger. 1987. PMID: 3111054 Danish. No abstract available.

8

Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and alpha 1-antitrypsin deficiency.

Nielsen JB, Güttler F, Hobolth N, Tønnesen T, Pedersen OD, Lykkelund C, Rosleff F. Nielsen JB, et al. Eur J Pediatr. 1986 Dec;145(6):572-5. doi: 10.1007/BF02429071. Eur J Pediatr. 1986. PMID: 2949978

9

Highly increased levels of serum beta-hexosaminidase, arylsulphatase A and beta-galactosidase in a patient with sepsis.

Tønnesen T, Andersen P, Güttler F. Tønnesen T, et al. J Inherit Metab Dis. 1988;11(4):428-9. doi: 10.1007/BF01800435. J Inherit Metab Dis. 1988. PMID: 2907595 No abstract available.

10

Feasibility of first trimester prenatal diagnosis of Hunter syndrome.

Lykkelund C, Søndergaard F, Therkelsen AJ, Tønnesen T, Rasmussen V, Mikkelsen M, Güttler F, Nyland MH. Lykkelund C, et al. Lancet. 1983 Nov 12;2(8359):1147. doi: 10.1016/s0140-6736(83)90665-7. Lancet. 1983. PMID: 6138678 No abstract available.

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