McCredie DA - Search Results

1

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.

Jaureguiberry G, De la Dure-Molla M, Parry D, Quentric M, Himmerkus N, Koike T, Poulter J, Klootwijk E, Robinette SL, Howie AJ, Patel V, Figueres ML, Stanescu HC, Issler N, Nicholson JK, Bockenhauer D, Laing C, Walsh SB, McCredie DA, Povey S, Asselin A, Picard A, Coulomb A, Medlar AJ, Bailleul-Forestier I, Verloes A, Le Caignec C, Roussey G, Guiol J, Isidor B, Logan C, Shore R, Johnson C, Inglehearn C, Al-Bahlani S, Schmittbuhl M, Clauss F, Huckert M, Laugel V, Ginglinger E, Pajarola S, Spartà G, Bartholdi D, Rauch A, Addor MC, Yamaguti PM, Safatle HP, Acevedo AC, Martelli-Júnior H, dos Santos Netos PE, Coletta RD, Gruessel S, Sandmann C, Ruehmann D, Langman CB, Scheinman SJ, Ozdemir-Ozenen D, Hart TC, Hart PS, Neugebauer U, Schlatter E, Houillier P, Gahl WA, Vikkula M, Bloch-Zupan A, Bleich M, Kitagawa H, Unwin RJ, Mighell A, Berdal A, Kleta R. Jaureguiberry G, et al. Among authors: mccredie da. Nephron Physiol. 2012;122(1-2):1-6. doi: 10.1159/000349989. Epub 2013 Feb 23. Nephron Physiol. 2012. PMID: 23434854 Free PMC article.

2

Ultrastructural study of tooth enamel with amelogenesis imperfecta in AI-nephrocalcinosis syndrome.

Phakey P, Palamara J, Hall RK, McCredie DA. Phakey P, et al. Among authors: mccredie da. Connect Tissue Res. 1995;32(1-4):253-9. doi: 10.3109/03008209509013731. Connect Tissue Res. 1995. PMID: 7554924

3

Amelogenesis imperfecta and nephrocalcinosis syndrome. Case studies of clinical features and ultrastructure of tooth enamel in two siblings.

Hall RK, Phakey P, Palamara J, McCredie DA. Hall RK, et al. Among authors: mccredie da. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1995 May;79(5):583-92. doi: 10.1016/s1079-2104(05)80100-3. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1995. PMID: 7600222

4

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor.

Pearce SH, Williamson C, Kifor O, Bai M, Coulthard MG, Davies M, Lewis-Barned N, McCredie D, Powell H, Kendall-Taylor P, Brown EM, Thakker RV. Pearce SH, et al. N Engl J Med. 1996 Oct 10;335(15):1115-22. doi: 10.1056/NEJM199610103351505. N Engl J Med. 1996. PMID: 8813042 Free article.

5

Familial hypomagnesaemia--hypercalciuria leading to end-stage renal failure.

Nicholson JC, Jones CL, Powell HR, Walker RG, McCredie DA. Nicholson JC, et al. Among authors: mccredie da. Pediatr Nephrol. 1995 Feb;9(1):74-6. doi: 10.1007/BF00858976. Pediatr Nephrol. 1995. PMID: 7742227

6

Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites.

Hannan FM, Nesbit MA, Zhang C, Cranston T, Curley AJ, Harding B, Fratter C, Rust N, Christie PT, Turner JJ, Lemos MC, Bowl MR, Bouillon R, Brain C, Bridges N, Burren C, Connell JM, Jung H, Marks E, McCredie D, Mughal Z, Rodda C, Tollefsen S, Brown EM, Yang JJ, Thakker RV. Hannan FM, et al. Hum Mol Genet. 2012 Jun 15;21(12):2768-78. doi: 10.1093/hmg/dds105. Epub 2012 Mar 14. Hum Mol Genet. 2012. PMID: 22422767

7

Computed tomographic assessment of vertebral bone mineral in childhood.

Fredericks BJ, de Campo JF, Sephton R, McCredie DA. Fredericks BJ, et al. Among authors: mccredie da. Skeletal Radiol. 1990;19(2):99-102. doi: 10.1007/BF00197613. Skeletal Radiol. 1990. PMID: 2321051

8

Paediatric cadaveric renal transplantation. Initial experience with a triple therapy immunosuppressive regimen.

Walker RG, d'Apice AJ, Powell HR, Francis DM, McCredie DA, Kincaid-Smith P. Walker RG, et al. Among authors: mccredie da. Pediatr Nephrol. 1987 Oct;1(4):611-4. doi: 10.1007/BF00853598. Pediatr Nephrol. 1987. PMID: 3153341

9

An extreme example of the neonatal form of Bartter's syndrome.

Williams MP, Jones CL, Johnstone LM, Walker RG, McCredie DA, Powell HR. Williams MP, et al. Among authors: mccredie da. Pediatr Nephrol. 1996 Aug;10(4):496-7. doi: 10.1007/s004670050147. Pediatr Nephrol. 1996. PMID: 8865251

10

Persistent familial hematuria in children and the locus for thin basement membrane nephropathy.

Rana K, Wang YY, Powell H, Jones C, McCredie D, Buzza M, Udawela M, Savige J. Rana K, et al. Pediatr Nephrol. 2005 Dec;20(12):1729-37. doi: 10.1007/s00467-005-2034-2. Epub 2005 Oct 19. Pediatr Nephrol. 2005. PMID: 16235097

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

42 results

Search Page

Filters