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Items: 1 to 50 of 96

1.

Prevention of food allergy in infants and children. Strategies under discussion.

Endres W.

Ann Nutr Metab. 2000;44(5-6):183-6. Review. No abstract available.

PMID:
11146321
3.

Diet in phenylketonuria: how long? Policies under discussion.

Endres W.

Ann Nutr Metab. 1998;42(2):63-7. Review. No abstract available.

PMID:
9625276
5.

Inherited metabolic diseases affecting the carrier.

Endres W.

J Inherit Metab Dis. 1997 Mar;20(1):9-20. Review.

PMID:
9061562
6.

No significant influence of HLA determinants on susceptibility to hepatitis C virus infection in Caucasian patients with end-stage renal disease.

Chen DF, Endres W, Kliem V, Tillmann HL, Brunkhorst R, Koch KM, Manns MP, Stangel W.

Liver. 1996 Dec;16(6):384-9.

PMID:
9021718
7.

Relationship between human leukocyte antigen determinants and courses of hepatitis B virus infection in Caucasian patients with end-stage renal disease.

Chen DF, Kliem V, Endres W, Brunkhorst R, Tillmann HL, Koch KM, Manns MP, Stangel W.

Scand J Gastroenterol. 1996 Dec;31(12):1211-5.

PMID:
8976014
8.

Simplified PCR-SSO procedure for DQA and DQB typing. Simultaneous hybridization of two probes to one membrane.

Chen DF, Endres W, Meyer SA, Stangel W.

Hum Immunol. 1996 Apr;46(2):120-3.

PMID:
8727211
10.

[Phenylketonuria and its treatment in and beyond adolescence].

Endres W.

Internist (Berl). 1994 Mar;35(3):250-4. Review. German. No abstract available.

PMID:
8175289
11.

[HLA-DR typing using PCR-SSO with simultaneous hybridization of each dot blot membrane with a digoxigenin- and a biotin-marked probe].

Chen DF, Endres W, Meyer SA, Stangel W.

Beitr Infusionsther Transfusionsmed. 1994;32:261-5. German.

PMID:
9480104
12.

[Familial investigations of carriers of Rh 33].

Endres W, Lichy S, Stangel W.

Beitr Infusionsther Transfusionsmed. 1994;32:187-9. German.

PMID:
9480082
14.

Parenteral administration of amino acids in disorders of branched-chain amino acid metabolism.

Sperl W, Skladal D, Endres W, Speer G, Groke K.

J Inherit Metab Dis. 1994;17(6):753-4. No abstract available.

PMID:
7707702
15.

Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria.

Ibel H, Endres W, Hadorn HB, Deufel T, Paetzke I, Duran M, Kennaway NG, Gibson KM.

Eur J Pediatr. 1993 Aug;152(8):665-70.

PMID:
7691603
16.

Hartnup syndrome, progressive encephalopathy and allo-albuminaemia. A clinico-pathological case study.

Schmidtke K, Endres W, Roscher A, Ibel H, Herschkowitz N, Bachmann C, Plöchl E, Hadorn HB.

Eur J Pediatr. 1992 Dec;151(12):899-903.

PMID:
1473543
17.

[Differential diagnosis and therapy of various forms of hyperphenylalaninemia: facts and fiction].

Endres W.

Wien Klin Wochenschr. 1992;104(16):503-9. Review. German.

PMID:
1413808
18.

Screening for tetrahydrobiopterin deficiency in newborns using dried urine on filter paper.

Blau N, Kierat L, Heizmann CW, Endres W, Giudici T, Wang M.

J Inherit Metab Dis. 1992;15(3):402-4. No abstract available.

PMID:
1405479
19.

Inadequate iron availability as a possible cause of low serum carnitine concentrations in patients with phenylketonuria.

Böhles H, Ullrich K, Endres W, Behbehani AW, Wendel U.

Eur J Pediatr. 1991 Apr;150(6):425-8.

PMID:
2040352
20.

[Treatment of glycogen storage diseases].

Endres WT.

Padiatr Padol. 1991;26(1):19-24. Review. German.

PMID:
1905390
21.

Bone marrow transplantation in Lesch-Nyhan disease.

Endres W, Helmig M, Shin YS, Albert E, Wank R, Ibel H, Weiss M, Hadorn HB, Hass R.

J Inherit Metab Dis. 1991;14(2):270-1. No abstract available.

PMID:
1886412
22.

Purification of alpha and beta subunits of phosphorylase-b-kinase in human liver and cardiac muscle by affinity chromatography and immunodetection.

Podskarbi T, Endres W, Shin YS.

J Inherit Metab Dis. 1991;14(3):308-10. No abstract available.

PMID:
1770779
23.

Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies.

Müller-Höcker J, Ibel H, Paetzke I, Deufel T, Endres W, Kadenbach B, Gokel JM, Hübner G.

Virchows Arch A Pathol Anat Histopathol. 1991;419(4):355-62.

PMID:
1659034
24.

[D-penicillamine-induced IgA deficiency in the therapy of Wilson's disease].

Ibel H, Feist D, Endres W, Belohradsky BH.

Klin Padiatr. 1990 Nov-Dec;202(6):427-9. German.

PMID:
2266710
25.

Alpha 1-antitrypsin deficiency and prune-belly syndrome--first report of coincidence.

Schmittenbecher PP, Endres W.

Klin Wochenschr. 1990 Mar 16;68(6):346. No abstract available.

PMID:
2335908
26.

Plasma polyol levels in patients with cataract.

Jakobs C, Douwes AC, Brockstedt M, Stellaard F, Endres W, Shin YS.

J Inherit Metab Dis. 1990;13(4):517-22.

PMID:
2122118
27.

Cataract and metabolic disease.

Endres W, Shin YS.

J Inherit Metab Dis. 1990;13(4):509-16. Review.

PMID:
2122117
28.

Progression of 6-pyruvoyl-tetrahydropterin synthase deficiency from a peripheral into a central phenotype.

Ponzone A, Blau N, Guardamagna O, Ferrero GB, Dianzani I, Endres W.

J Inherit Metab Dis. 1990;13(3):298-300. No abstract available.

PMID:
1700190
29.

Acetylcholinesterase reactivators antagonize epileptiform bursting induced by paraoxon in guinea pig hippocampal slices.

Endres W, Spuler A, ten Bruggencate G.

J Pharmacol Exp Ther. 1989 Dec;251(3):1181-6.

PMID:
2600810
30.

Electrophysiological recordings of changes in relative cell volume of neurones, glia, and muscle cells.

Ballanyi K, Serve G, Endres W, Strupp M, Grafe P.

Acta Physiol Scand Suppl. 1989;582:25. No abstract available.

PMID:
2816429
31.

First trimester diagnosis of glycogen storage disease type II and type III.

Shin YS, Rieth M, Tausenfreund J, Endres W.

J Inherit Metab Dis. 1989;12 Suppl 2:289-91. No abstract available.

PMID:
2512428
32.

Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency.

Endres W, Shin YS, Günther R, Ibel H, Duran M, Wadman SK.

Eur J Pediatr. 1988 Dec;148(3):246-9.

PMID:
3215199
33.

Clinical course of hereditary fructose intolerance in 56 patients.

Endres W, Sierck T, Shin YS.

Acta Paediatr Jpn. 1988 Aug;30(4):452-6. No abstract available.

PMID:
3150235
34.

Elevated plasma galactitol levels in patients with congenital cataracts without apparent enzyme defect.

Jakobs C, Douwes AC, Kok R, de Jong A, Endres W, Shin YS.

Eur J Pediatr. 1988 May;147(4):446. No abstract available.

PMID:
3396605
35.
36.
37.

Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotes.

Shin YS, Steigüber H, Klemm P, Endres W, Schwab O, Wolff G.

J Inherit Metab Dis. 1988;11 Suppl 2:252-4. No abstract available.

PMID:
2972882
38.

Priapism in Fabry's disease during testosterone treatment.

Endres W, Shin YS, Rieth M, Block T, Schmiedt E, Knorr D.

Klin Wochenschr. 1987 Oct 1;65(19):925. No abstract available.

PMID:
3123767
39.

Tetrahydrobiopterin and "non-responsive" dihydropteridine reductase deficiency.

Endres W, Ibel H, Kierat L, Blau N, Curtius HC.

Lancet. 1987 Jul 25;2(8552):223. No abstract available.

PMID:
2885683
40.
41.

"Peripheral" tetrahydrobiopterin deficiency with hyperphenylalaninaemia due to incomplete 6-pyruvoyl tetrahydropterin synthase deficiency or heterozygosity.

Niederwieser A, Shintaku H, Leimbacher W, Curtius HC, Hyànek J, Zeman J, Endres W.

Eur J Pediatr. 1987 May;146(3):228-32.

PMID:
3297709
42.
43.

Increased concentrations of HbAlab in hereditary fructose intolerance and galactosemia.

Böhles H, Schädle J, Endres W, Shin YS, Kollmann F, Bender SW, Kruse K.

Padiatr Padol. 1987;22(1):25-31.

PMID:
3587991
44.

Excitatory amino acids and intracellular pH in motoneurons of the isolated frog spinal cord.

Endres W, Ballanyi K, Serve G, Grafe P.

Neurosci Lett. 1986 Dec 3;72(1):54-8.

PMID:
2880318
45.
46.

Changes in extracellular pH during electrical stimulation of isolated rat vagus nerve.

Endres W, Grafe P, Bostock H, ten Bruggencate G.

Neurosci Lett. 1986 Feb 28;64(2):201-5.

PMID:
2421206
47.
48.

Pyridoxal-5'-phosphate concentration as marker for vitamin-B6-dependent seizures in the newborn.

Shin YS, Rasshofer R, Endres W.

Lancet. 1984 Oct 13;2(8407):870-1. No abstract available.

PMID:
6148599
49.

A simple assay for amylo-1,6-glucosidase to detect heterozygotes for glycogenosis type III in erythrocytes.

Shin YS, Ungar R, Rieth M, Endres W.

Clin Chem. 1984 Oct;30(10):1717-8. No abstract available.

50.

Glycosylated haemoglobin and glycosylated albumin: evaluation of different methods in diabetic control.

Shin YS, Stern C, von Rücker A, Endres W.

J Clin Chem Clin Biochem. 1984 Jan;22(1):47-51.

PMID:
6699551

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