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NEUROLOGY MCQ – Exercise 60

The multiple choice questions in this online test paper focuses on NEUROLOGY MCQ. If you are looking for self evaluation of your PG Medical entrance exam preparation then this online NEUROLOGY MCQ Test Paper will help you to evaluate your exam preparation.


1- This online MCQ practice test paper contains 30 questions.
2- Each question in this online practice test paper have four options and only 1 option is correct.
3- You can view the answers of this practice test paper after submitting the practice test paper.
Note: The answers mentioned at the end of practice test are the best suitable option as per our knowledge. Users shall cross-check the answers with their textbooks.

Q 1. regarding lipid as a source of energy which is true


Q 2. disorder of glycolysis causing exercise intolerance


Q 3. acyl-CoA must be linked to which of the following for transport into mitochondria


Q 4. MELAS include all except


Q 5. MELAS include all except


Q 6. maternally inherited point mutations of mitochondrial tRNA gene


Q 7. twinkle is the gene product of


Q 8. most common alpha glucosidase or acid maltase deficiency form


Q 9. which is caused by maternally inherited point mutations of mitochondrial tRNA gene


Q 10. characteristic feature of myoclonic epilepsy with ragged red fibers is (MERRF) is


Q 11. following point mutation is most common in MELAS


Q 12. enzyme important in mtDNA replication is


Q 13. Kearns Sayre syndrome includes all except


Q 14. progressive external ophthalmoplegia includes all except


Q 15. mitochondrial myopathy includes


Q 16. x linked recessive disorder includes


Q 17. potassium channelopathy includes


Q 18. Pompe`s disease includes


Q 19. McArdle`s diseaseis also called


Q 20. carnitine palmitoyltransferase II is present on


Q 21. cardinal signs of mitochondrial disorders


Q 22. to enter mitochondria fatty acid must first be converted to


Q 23. ragged red fibers is muscle cell with significant numbers of abnormal


Q 24. myoglobinuria in carnitine palmitoyltransferase II deficiency is precipitated by


Q 25. human mitochondrial DNA includes


Q 26. carnitine palmitoyltransferase I is present on


Q 27. seizure disorder with mental retardation is a feature of


Q 28. Kearns Sayre syndrome includes all except


Q 29. chromosome is affected in autosomal dominant form of CPEO


Q 30. calcium channelopathy includes


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