Seyberth HW - Search Results

1

Dihydropyrimidinase deficiency and congenital microvillous atrophy: coincidence or genetic relation?

Assmann B, Hoffmann GF, Wagner L, Bräutigam C, Seyberth HW, Duran M, Van Kuilenburg AB, Wevers R, Van Gennip AH. Assmann B, et al. Among authors: seyberth hw. J Inherit Metab Dis. 1997 Sep;20(5):681-8. doi: 10.1023/a:1005374426168. J Inherit Metab Dis. 1997. PMID: 9323563

2

Severe hyperchloriduria-hyperkaliuria: a new congenital renal tubular abnormality?

Meyburg J, Mayatepek E, Hoffmann GF, Linderkamp O, Seyberth HW. Meyburg J, et al. Among authors: seyberth hw. J Pediatr. 1996 Mar;128(3):376-8. doi: 10.1016/s0022-3476(96)70286-x. J Pediatr. 1996. PMID: 8774509

3

Severe hyperprostaglandin E syndrome with hyperthyroidism--studies of pathogenetic mechanisms.

Fellman V, Pihko H, Majander A, Seyberth HW. Fellman V, et al. Among authors: seyberth hw. J Inherit Metab Dis. 1996;19(5):687-94. doi: 10.1007/BF01799846. J Inherit Metab Dis. 1996. PMID: 8892027

4

The molecular genetic approach to "Bartter's syndrome".

Károlyi L, Koch MC, Grzeschik KH, Seyberth HW. Károlyi L, et al. Among authors: seyberth hw. J Mol Med (Berl). 1998 Apr;76(5):317-25. doi: 10.1007/s001090050223. J Mol Med (Berl). 1998. PMID: 9587066 Review.

5

Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness.

Jeck N, Reinalter SC, Henne T, Marg W, Mallmann R, Pasel K, Vollmer M, Klaus G, Leonhardt A, Seyberth HW, Konrad M. Jeck N, et al. Among authors: seyberth hw. Pediatrics. 2001 Jul;108(1):E5. doi: 10.1542/peds.108.1.e5. Pediatrics. 2001. PMID: 11433084

6

Impaired response to furosemide in hyperprostaglandin E syndrome: evidence for a tubular defect in the loop of Henle.

Köckerling A, Reinalter SC, Seyberth HW. Köckerling A, et al. Among authors: seyberth hw. J Pediatr. 1996 Oct;129(4):519-28. doi: 10.1016/s0022-3476(96)70116-6. J Pediatr. 1996. PMID: 8859258 Clinical Trial.

7

Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene.

Weber S, Hoffmann K, Jeck N, Saar K, Boeswald M, Kuwertz-Broeking E, Meij II, Knoers NV, Cochat P, Suláková T, Bonzel KE, Soergel M, Manz F, Schaerer K, Seyberth HW, Reis A, Konrad M. Weber S, et al. Among authors: seyberth hw. Eur J Hum Genet. 2000 Jun;8(6):414-22. doi: 10.1038/sj.ejhg.5200475. Eur J Hum Genet. 2000. PMID: 10878661

8

Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes.

Konrad M, Leonhardt A, Hensen P, Seyberth HW, Köckerling A. Konrad M, et al. Among authors: seyberth hw. Pediatrics. 1999 Mar;103(3):678-83. doi: 10.1542/peds.103.3.678. Pediatrics. 1999. PMID: 10049979

9

Biosynthesis of prostacyclin and thromboxane A2 during chronic hypoxaemia in children with cyanotic congenital heart disease.

Leonhardt A, Magsaam J, Goldner M, Kühl PG, Seyberth HW. Leonhardt A, et al. Among authors: seyberth hw. Eur J Clin Invest. 1996 Dec;26(12):1057-61. doi: 10.1046/j.1365-2362.1996.370590.x. Eur J Clin Invest. 1996. PMID: 9013079

10

Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome.

Károlyi L, Ziegler A, Pollak M, Fischbach M, Grzeschik KH, Koch MC, Seyberth HW. Károlyi L, et al. Among authors: seyberth hw. Pediatr Nephrol. 1996 Oct;10(5):551-4. doi: 10.1007/s004670050158. Pediatr Nephrol. 1996. PMID: 8897553

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