Ruitenbeek W - Search Results

1

Positron emission tomography and magnetic resonance spectroscopy of cerebral glycolysis in children with congenital lactic acidosis.

Duncan DB, Herholz K, Kugel H, Roth B, Ruitenbeek W, Heindel W, Wienhard K, Heiss WD. Duncan DB, et al. Among authors: ruitenbeek w. Ann Neurol. 1995 Mar;37(3):351-8. doi: 10.1002/ana.410370311. Ann Neurol. 1995. PMID: 7695234 Free article.

2

Proton spectroscopy in five patients with Leigh's disease and mitochondrial enzyme deficiency.

Krägeloh-Mann I, Grodd W, Schöning M, Marquard K, Nägele T, Ruitenbeek W. Krägeloh-Mann I, et al. Among authors: ruitenbeek w. Dev Med Child Neurol. 1993 Sep;35(9):769-76. doi: 10.1111/j.1469-8749.1993.tb11728.x. Dev Med Child Neurol. 1993. PMID: 7689066

3

Assessment and therapy monitoring of Leigh disease by MRI and proton spectroscopy.

Krägeloh-Mann I, Grodd W, Niemann G, Haas G, Ruitenbeek W. Krägeloh-Mann I, et al. Among authors: ruitenbeek w. Pediatr Neurol. 1992 Jan-Feb;8(1):60-4. doi: 10.1016/0887-8994(92)90055-4. Pediatr Neurol. 1992. PMID: 1558578

4

A mitochondrial myopathy in an infant with lactic acidosis.

Griebel V, Krägeloh-Mann I, Ruitenbeek W, Trijbels JM, Paulus W. Griebel V, et al. Among authors: ruitenbeek w. Dev Med Child Neurol. 1990 Jun;32(6):528-31. doi: 10.1111/j.1469-8749.1990.tb16979.x. Dev Med Child Neurol. 1990. PMID: 2365146

5

Mitochondrial encephalomyopathy, lactic acidosis and stroke in adults: two cases.

Kremer HP, Keyser A, Wintzen AR, Scholte HR, van Hellenberg Hubar JG, Poorthuis BJ, Ruitenbeek W. Kremer HP, et al. Among authors: ruitenbeek w. J Neurol. 1993;240(4):219-22. doi: 10.1007/BF00818708. J Neurol. 1993. PMID: 8496710

6

New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiency.

Dionisi-Vici C, Ruitenbeek W, Fariello G, Bentlage H, Wanders RJ, Schägger H, Bosman C, Piantadosi C, Sabetta G, Bertini E. Dionisi-Vici C, et al. Among authors: ruitenbeek w. Ann Neurol. 1997 Oct;42(4):661-5. doi: 10.1002/ana.410420419. Ann Neurol. 1997. PMID: 9382480 Free article.

7

In vivo methods useful for therapy monitoring in lactic acidosis.

Schulze A, Mayatepek E, Langhans CD, Bachert P, Ruitenbeek W, Rating D. Schulze A, et al. Among authors: ruitenbeek w. J Inherit Metab Dis. 1998 Aug;21(6):691-2. doi: 10.1023/a:1005409323161. J Inherit Metab Dis. 1998. PMID: 9762614 No abstract available.

8

Mitochondrial angiopathy in a family with MELAS.

Förster C, Hübner G, Müller-Höcker J, Pongratz D, Baierl P, Senger R, Ruitenbeek W. Förster C, et al. Among authors: ruitenbeek w. Neuropediatrics. 1992 Jun;23(3):165-8. doi: 10.1055/s-2008-1071335. Neuropediatrics. 1992. PMID: 1322508

9

A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome.

De Coo IF, Renier WO, Ruitenbeek W, Ter Laak HJ, Bakker M, Schägger H, Van Oost BA, Smeets HJ. De Coo IF, et al. Among authors: ruitenbeek w. Ann Neurol. 1999 Jan;45(1):130-3. doi: 10.1002/1531-8249(199901)45:1<130::aid-art21>3.3.co;2-q. Ann Neurol. 1999. PMID: 9894888

10

Adenine nucleotide translocator 1 deficiency associated with Sengers syndrome.

Jordens EZ, Palmieri L, Huizing M, van den Heuvel LP, Sengers RC, Dörner A, Ruitenbeek W, Trijbels FJ, Valsson J, Sigfusson G, Palmieri F, Smeitink JA. Jordens EZ, et al. Among authors: ruitenbeek w. Ann Neurol. 2002 Jul;52(1):95-9. doi: 10.1002/ana.10214. Ann Neurol. 2002. PMID: 12112053

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

150 results

Search Page

Filters