Naidu S - Search Results

1

Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism.

Danpure CJ, Fryer P, Griffiths S, Guttridge KM, Jennings PR, Allsop J, Moser AB, Naidu S, Moser HW, MacCollin M, et al. Danpure CJ, et al. Among authors: naidu s. J Inherit Metab Dis. 1994;17(1):27-40. doi: 10.1007/BF00735393. J Inherit Metab Dis. 1994. PMID: 8051936

2

Peroxisomal disorders.

Naidu S, Moser HW. Naidu S, et al. Neurol Clin. 1990 Aug;8(3):507-28. Neurol Clin. 1990. PMID: 2215454 Review.

3

Peroxisomal disorders.

Naidu S, Moser HW. Naidu S, et al. Neurol Clin. 1994 Nov;12(4):727-39. Neurol Clin. 1994. PMID: 7845339 Review.

4

Adrenoleukodystrophy: biochemical procedures in diagnosis, prevention and treatment.

Watkins PA, Naidu S, Moser HW. Watkins PA, et al. Among authors: naidu s. J Inherit Metab Dis. 1987;10 Suppl 1:46-53. doi: 10.1007/BF01812846. J Inherit Metab Dis. 1987. PMID: 3119941 Review.

5

Phenotypic and genotypic variability of generalized peroxisomal disorders.

Naidu S, Moser AE, Moser HW. Naidu S, et al. Pediatr Neurol. 1988 Jan-Feb;4(1):5-12. doi: 10.1016/0887-8994(88)90017-3. Pediatr Neurol. 1988. PMID: 3069099 Review.

6

Infantile Refsum disease.

Naidu S, Moser H. Naidu S, et al. AJNR Am J Neuroradiol. 1991 Nov-Dec;12(6):1161-3. AJNR Am J Neuroradiol. 1991. PMID: 1722385 Free PMC article. No abstract available.

7

Cherry red spot in association with galactosylceramide-beta-galactosidase deficiency.

Hofman KJ, Naidu S, Moser HW, Maumenee IH, Wenger DA. Hofman KJ, et al. Among authors: naidu s. J Inherit Metab Dis. 1987;10(3):273-4. doi: 10.1007/BF01800078. J Inherit Metab Dis. 1987. PMID: 3123790 No abstract available.

8

Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls.

Moser AB, Kreiter N, Bezman L, Lu S, Raymond GV, Naidu S, Moser HW. Moser AB, et al. Among authors: naidu s. Ann Neurol. 1999 Jan;45(1):100-10. doi: 10.1002/1531-8249(199901)45:1<100::aid-art16>3.0.co;2-u. Ann Neurol. 1999. PMID: 9894883

9

Neuronal migration abnormality in peroxisomal bifunctional enzyme defect.

Kaufmann WE, Theda C, Naidu S, Watkins PA, Moser AB, Moser HW. Kaufmann WE, et al. Among authors: naidu s. Ann Neurol. 1996 Feb;39(2):268-71. doi: 10.1002/ana.410390218. Ann Neurol. 1996. PMID: 8967760

10

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups.

Moser AB, Rasmussen M, Naidu S, Watkins PA, McGuinness M, Hajra AK, Chen G, Raymond G, Liu A, Gordon D, et al. Moser AB, et al. Among authors: naidu s. J Pediatr. 1995 Jul;127(1):13-22. doi: 10.1016/s0022-3476(95)70250-4. J Pediatr. 1995. PMID: 7541833

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