198 results on '"ter Laak, H J"'
Search Results
2. Myopathology in patients with a Noonan phenotype
3. Congenital muscular dystrophy and severe central nervous system atrophy in two siblings
4. Anti-signal recognition particle autoantibodies: marker of a necrotising myopathy
5. Congenital muscular dystrophy: A study on the variability of morphological changes and dystrophin distribution in muscle biopsies
6. Histology of hereditary neuralgic amyotrophy
7. Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity
8. Diagnostic value of MHC class I staining in idiopathic inflammatory myopathies
9. Neuropathological findings in muscle-eye-brain disease (MEB-D): Neuropathological delineation of MEB-D from congenital muscular dystrophy of the Fukuyama type
10. A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions
11. Anti-Jo-1 positive inclusion body myositis with a marked and sustained clinical improvement after oral prednisone
12. Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle
13. Ia-Presenting Cells in early Multiple Sclerosis Lesions and Adjacent Normal Looking White Matter; A Morphological Study
14. Monoclonal Antibodies Against Oligodendrocytes; A Morphological Study
15. The effect of monoclonal anti-T cell antibodies on the clinical course of experimental allergic encephalomyelitis in rats
16. Polyglucosan bodies in intramuscular motor nerves
17. Successful carnitine treatment in a non-carnitine-deficient lipid storage myopathy
18. A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q
19. Kearns syndrome: A heterogeneous group of disorders with CPEO, or a nosological entity?
20. Galanin-like immunoreactivity within Ch2 neurons in the vertical limb of the diagonal band of Broca in aging and Alzheimer's disease
21. Functional classification of cells in the optic tract of a tree shrew (Tupaia chinensis)
22. Dysmyelination and disturbed metabolism of pyruvate: a case report
23. Maintained activity of cells in the tree shrew's optic tract
24. A mitochondrial myopathy with a defective respiratory chain and carnitine deficiency
25. Invariances of the Cone-Dominated ERG (Tree Shrew and Man)
26. Deficiency of cytochromes b and aa3 in muscle from a floppy infant with cytochrome oxidase deficiency
27. Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?
28. Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders
29. Primary respiratory failure in inclusion body myositis
30. Hypovitaminosis D-Related Myopathy in Immigrant Teenagers
31. Reply
32. A 4-base pair deletion in the mitochondrial cytochromeb gene associated with parkinsonism/MELAS overlap syndrome
33. Genetic characteristics of myoadenylate deaminase deficiency
34. Complex regional pain syndrome type I (RSD): Pathology of skeletal muscle and peripheral nerve
35. Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle
36. The Olfactory Bulb in Alzheimer Disease
37. Deficiency of Na+/K+-ATPase and sarcoplasmic reticulum Ca2+-ATPase in skeletal muscle and cultured muscle cells of myotonic dystrophy patients
38. Mitochondrial Myopathy or Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)?-Reply
39. FORCE AND FATIGUE IN HUMAN TYPE I MUSCLE FIBRES: A SURFACE EMG STUDY IN PATIENTS WITH CONGENITAL MYOPATHY AND TYPE I FIBRE PREDOMINANCE
40. A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome.
41. MELAS Syndrome - Report of Two Patients, and Comparison with Data of 24 Patients Derived from the Literature*.
42. Generalized Hypertrophic Myopathy Associated with Chorioretinal Dystrophy and Struma Lymphomatosa - A Case Report.
43. Peripheral and Central Myelinopathy in Cockayne's Syndrome. Report of 3 Siblings.
44. Multicore myopathy with restrictive cardiomyopathy.
45. Congenital Muscular Dystrophy with Eye and Brain Malformations in Six Dutch Patients*.
46. Influence of cerebroside and ganglioside on the encephalitogenic activity of myelin basic protein in guinea pigs.
47. A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle.
48. The rigid spine syndrome.
49. Chronic inflammatory demyelinating polyneuropathy in two siblings.
50. Kearns-Sayre syndrome Remarks on the pathogenesis with reference to a case with dwarfism and calcification of basal ganglia.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.