These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
75 related articles for article (PubMed ID: 8989468)
21. Neonatal seizures and limb malformations associated with liver-specific complex IV respiratory chain deficiency. Kurian MA; O'Mahoney ES; Rustin P; Brown G; Treacy EP; King MD Eur J Paediatr Neurol; 2004; 8(1):55-9. PubMed ID: 15023375 [TBL] [Abstract][Full Text] [Related]
22. New syndrome or severe expression of Gordon syndrome? A case report. Courtens W; Perlmutter N; Dan B; Vamos E Clin Dysmorphol; 1997 Jan; 6(1):39-44. PubMed ID: 9018417 [TBL] [Abstract][Full Text] [Related]
23. Multiple congenital anomalies/mental retardation syndrome with multiple circumferential skin creases: a new syndrome? Tinsa F; Aissa K; Meddeb M; Bousnina D; Boussetta K; Bousnina S J Child Neurol; 2009 Feb; 24(2):224-7. PubMed ID: 19182162 [TBL] [Abstract][Full Text] [Related]
24. Frequency of associated anomalies in congenital hypoplasia of depressor anguli oris muscle: a study of 50 patients. Lin DS; Huang FY; Lin SP; Chen MR; Kao HA; Hung HY; Hsu CH Am J Med Genet; 1997 Aug; 71(2):215-8. PubMed ID: 9217225 [TBL] [Abstract][Full Text] [Related]
25. Diagnostic yield muscle biopsy in patients with clinical evidence of mitochondrial cytopathy. Rollins S; Prayson RA; McMahon JT; Cohen BH Am J Clin Pathol; 2001 Sep; 116(3):326-30. PubMed ID: 11554158 [TBL] [Abstract][Full Text] [Related]
26. Clinical features and neuroradiological findings of mitochondrial pathology in six neonates. Gire C; Girard N; Nicaise C; Einaudi MA; Montfort MF; Dejode JM Childs Nerv Syst; 2002 Nov; 18(11):621-8. PubMed ID: 12420122 [TBL] [Abstract][Full Text] [Related]
27. Partial trisomy of the distal part of 10q: a report of two Egyptian cases. Aglan MS; Kamel AK; Helmy NA Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995 [TBL] [Abstract][Full Text] [Related]
28. Analysis of coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromes. Montero R; Sánchez-Alcázar JA; Briones P; Hernández AR; Cordero MD; Trevisson E; Salviati L; Pineda M; García-Cazorla A; Navas P; Artuch R Clin Biochem; 2008 Jun; 41(9):697-700. PubMed ID: 18387363 [TBL] [Abstract][Full Text] [Related]
29. Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples. Wiedemann FR; Vielhaber S; Schröder R; Elger CE; Kunz WS Anal Biochem; 2000 Mar; 279(1):55-60. PubMed ID: 10683230 [TBL] [Abstract][Full Text] [Related]
30. Normal muscle respiratory chain enzymes can complicate mitochondrial disease diagnosis. Oglesbee D; Freedenberg D; Kramer KA; Anderson BD; Hahn SH Pediatr Neurol; 2006 Oct; 35(4):289-92. PubMed ID: 16996407 [TBL] [Abstract][Full Text] [Related]
31. Two sisters with growth failure, microcephaly, peculiar facies and apical dystrophy: the presentation of brachymorphism-onychodysplasia-dysphalangism syndrome? Ounap K; Justus I; Lipping-Sitska M Clin Dysmorphol; 1998 Jan; 7(1):45-50. PubMed ID: 9546830 [TBL] [Abstract][Full Text] [Related]
32. Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities in skeletal muscle. Enns GM; Hoppel CL; DeArmond SJ; Schelley S; Bass N; Weisiger K; Horoupian D; Packman S Clin Genet; 2005 Oct; 68(4):337-48. PubMed ID: 16143021 [TBL] [Abstract][Full Text] [Related]
33. Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates. Honzik T; Wenchich L; Böhm M; Hansikova H; Pejznochova M; Zapadlo M; Plavka R; Zeman J Early Hum Dev; 2008 Apr; 84(4):269-76. PubMed ID: 17698302 [TBL] [Abstract][Full Text] [Related]
34. Ocular anomalies associated with interstitial deletion of chromosome 2q31: case report and review. Gambrelle J; Till M; Lukusa B; Beby F; Mory N; Sann L; Kodjikian L; Grange JD; Putet G Ophthalmic Genet; 2007 Jun; 28(2):105-9. PubMed ID: 17558854 [TBL] [Abstract][Full Text] [Related]