Böhles H - Search Results

1

Hyperinsulinaemic hypoglycaemia--leading symptom in a patient with congenital disorder of glycosylation Ia (phosphomannomutase deficiency).

Böhles H, Sewell AA, Gebhardt B, Reinecke-Lüthge A, Klöppel G, Marquardt T. Böhles H, et al. J Inherit Metab Dis. 2001 Dec;24(8):858-62. doi: 10.1023/a:1013944308881. J Inherit Metab Dis. 2001. PMID: 11916319

2

N-carbamylglutamate protects patients with decompensated propionic aciduria from hyperammonaemia.

Gebhardt B, Dittrich S, Parbel S, Vlaho S, Matsika O, Bohles H. Gebhardt B, et al. Among authors: bohles h. J Inherit Metab Dis. 2005;28(2):241-4. doi: 10.1007/s10545-005-5260-7. J Inherit Metab Dis. 2005. PMID: 15877213

3

[Present limitations of molecular biological diagnostics in Gillespie syndrome].

Kieslich M, Vanselow K, Wildhardt G, Gebhardt B, Weis R, Böhles H. Kieslich M, et al. Among authors: bohles h. Klin Padiatr. 2001 Mar-Apr;213(2):47-9. doi: 10.1055/s-2001-12875. Klin Padiatr. 2001. PMID: 11305191 German.

4

Reflections about possible nutritional supplements in infant milk formula.

Böhles H, Gebhardt B, Beeg T. Böhles H, et al. Z Ernahrungswiss. 1998 Jun;37(2):132-46. doi: 10.1007/pl00007375. Z Ernahrungswiss. 1998. PMID: 9698641 Review.

5

Carnitine esters in metabolic disease.

Böhles H, Evangeliou A, Bervoets K, Eckert I, Sewell A. Böhles H, et al. Eur J Pediatr. 1994;153(7 Suppl 1):S57-61. doi: 10.1007/BF02138779. Eur J Pediatr. 1994. PMID: 7957388 Review. No abstract available.

6

Maternal plasma homocysteine, placenta status and docosahexaenoic acid concentration in erythrocyte phospholipids of the newborn.

Böhles H, Arndt S, Ohlenschläger U, Beeg T, Gebhardt B, Sewell AC. Böhles H, et al. Eur J Pediatr. 1999 Mar;158(3):243-6. doi: 10.1007/s004310051059. Eur J Pediatr. 1999. PMID: 10094448

7

[Diagnostic difficulties in encephalitis and glioma].

Parbel S, Vlaho S, Gebhardt B, Porto L, Hattingen E, Klingebiel T, Böhles H, Kieslich M. Parbel S, et al. Among authors: bohles h. Klin Padiatr. 2007 Jul-Aug;219(4):222-4. doi: 10.1055/s-2006-933521. Epub 2006 Jul 24. Klin Padiatr. 2007. PMID: 16865652 German.

8

alpha-Lipoic acid treatment decreases serum lactate and pyruvate concentrations and improves glucose effectiveness in lean and obese patients with type 2 diabetes.

Konrad T, Vicini P, Kusterer K, Höflich A, Assadkhani A, Böhles HJ, Sewell A, Tritschler HJ, Cobelli C, Usadel KH. Konrad T, et al. Among authors: bohles hj. Diabetes Care. 1999 Feb;22(2):280-7. doi: 10.2337/diacare.22.2.280. Diabetes Care. 1999. PMID: 10333946

9

Mitochondrial respiratory chain succinate-cytochrome-c oxidoreductase deficiency and hepatic cirrhosis.

Sewell AC, Herwig J, Böhles HJ, Sperl W. Sewell AC, et al. Among authors: bohles hj. J Inherit Metab Dis. 1997 Nov;20(6):837-8. doi: 10.1023/a:1005392406628. J Inherit Metab Dis. 1997. PMID: 9427157 No abstract available.

10

Early signs and course of disease of glutaryl-CoA dehydrogenase deficiency.

Hoffmann GF, Böhles HJ, Burlina A, Duran M, Herwig J, Lehnert W, Leonard JV, Muntau A, Plecko-Starting FK, Superti-Furga A, et al. Hoffmann GF, et al. Among authors: bohles hj. J Inherit Metab Dis. 1995;18(2):173-6. doi: 10.1007/BF00711759. J Inherit Metab Dis. 1995. PMID: 7564239 No abstract available.

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