PubMed (cited) for id: 134600

Year	Number of Results
1951	1
1955	1
1956	1
1957	1
1961	2
1976	1
1978	2
1981	2
1989	1
1990	1
1991	1
1992	1
2000	1
2001	1
2018	1
2024	0

1

Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.

Reichold M, Klootwijk ED, Reinders J, Otto EA, Milani M, Broeker C, Laing C, Wiesner J, Devi S, Zhou W, Schmitt R, Tegtmeier I, Sterner C, Doellerer H, Renner K, Oefner PJ, Dettmer K, Simbuerger JM, Witzgall R, Stanescu HC, Dumitriu S, Iancu D, Patel V, Mozere M, Tekman M, Jaureguiberry G, Issler N, Kesselheim A, Walsh SB, Gale DP, Howie AJ, Martins JR, Hall AM, Kasgharian M, O'Brien K, Ferreira CR, Atwal PS, Jain M, Hammers A, Charles-Edwards G, Choe CU, Isbrandt D, Cebrian-Serrano A, Davies B, Sandford RN, Pugh C, Konecki DS, Povey S, Bockenhauer D, Lichter-Konecki U, Gahl WA, Unwin RJ, Warth R, Kleta R. Reichold M, et al. J Am Soc Nephrol. 2018 Jul;29(7):1849-1858. doi: 10.1681/ASN.2017111179. Epub 2018 Apr 13. J Am Soc Nephrol. 2018. PMID: 29654216 Free PMC article.

2

The genetics of cystinuria.

DENT CE, HARRIS H. DENT CE, et al. Ann Eugen. 1951 Jul;16(1):60-87. doi: 10.1111/j.1469-1809.1951.tb02459.x. Ann Eugen. 1951. PMID: 24541401 No abstract available.

3

A Familial Tubular Absorption Defect of Glucose and Amino Acids.

Sheldon W, Luder J, Webb B. Sheldon W, et al. Arch Dis Child. 1961 Feb;36(185):90-5. doi: 10.1136/adc.36.185.90. Arch Dis Child. 1961. PMID: 21032379 Free PMC article. No abstract available.

4

A familial tubular absorption defect of glucose and amino acids.

LUDER J, SHELDON W. LUDER J, et al. Arch Dis Child. 1955 Apr;30(150):160-4. doi: 10.1136/adc.30.150.160. Arch Dis Child. 1955. PMID: 14377624 Free PMC article. No abstract available.

5

Fanconi syndrome with hypouricemia in an adult: family study.

BEN-ISHAY D, DREYFUSS F, ULLMANN TD. BEN-ISHAY D, et al. Am J Med. 1961 Nov;31:793-800. doi: 10.1016/0002-9343(61)90163-2. Am J Med. 1961. PMID: 13867012 No abstract available.

6

The adult Fanconi syndrome. II. Review of eighteen cases.

ENGLE RL Jr, WALLIS LA. ENGLE RL Jr, et al. Am J Med. 1957 Jan;22(1):13-23. Am J Med. 1957. PMID: 13381735 No abstract available.

7

Hereditary forms of rickets and osteomalacia.

DENT CE, HARRIS H. DENT CE, et al. J Bone Joint Surg Br. 1956 Feb;38-B(1):204-26. doi: 10.1302/0301-620X.38B1.204. J Bone Joint Surg Br. 1956. PMID: 13295329 No abstract available.

8

Genetic and physical mapping of the locus for autosomal dominant renal Fanconi syndrome, on chromosome 15q15.3.

Lichter-Konecki U, Broman KW, Blau EB, Konecki DS. Lichter-Konecki U, et al. Am J Hum Genet. 2001 Jan;68(1):264-8. doi: 10.1086/316923. Epub 2000 Nov 22. Am J Hum Genet. 2001. PMID: 11090339 Free PMC article.

9

A family with a dominant form of idiopathic Fanconi syndrome leading to renal failure in adult life.

Patrick A, Cameron JS, Ogg CS. Patrick A, et al. Clin Nephrol. 1981 Dec;16(6):289-92. Clin Nephrol. 1981. PMID: 7032774

10

The adult presenting idiopathic Fanconi syndrome.

Brenton DP, Isenberg DA, Cusworth DC, Garrod P, Krywawych S, Stamp TC. Brenton DP, et al. J Inherit Metab Dis. 1981;4(4):211-5. doi: 10.1007/BF02263654. J Inherit Metab Dis. 1981. PMID: 6796773

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