-
1
-
-
33746486177
-
Medullary sponge kidney associated with distal renal tubular acidosis in a 5-year-old girl
-
DOI 10.1007/s00431-006-0125-0
-
Kasap B, Soylu A, Oren O, Türkmen M, Kavukçu S: Medullary sponge kidney associated with distal renal tubular acidosis in a 5-year-old girl. Eur J Pediatr 165: 648-651, 2006 (Pubitemid 44134227)
-
(2006)
European Journal of Pediatrics
, vol.165
, Issue.9
, pp. 648-651
-
-
Kasap, B.1
Soylu, A.2
Oren, O.3
Turkmen, M.4
Kavukcu, S.5
-
3
-
-
32544436448
-
Medullary sponge kidney
-
3rd Ed., edited by Davison AM, Cameron JS, Grunfeld J-P, Ponticelli C, Ritz E, Winearls CG, van Ypersele C, Oxford University Press, Oxford, United Kingdom
-
Cameron S: Medullary sponge kidney. In: Oxford Textbook of Clinical Nephrology, 3rd Ed., edited by Davison AM, Cameron JS, Grunfeld J-P, Ponticelli C, Ritz E, Winearls CG, van Ypersele C, Oxford University Press, Oxford, United Kingdom, 2004, pp 2495-2501
-
(2004)
Oxford Textbook of Clinical Nephrology
, pp. 2495-2501
-
-
Cameron, S.1
-
4
-
-
0023217667
-
Medullary sponge disease in horseshoe kidney
-
Lambrianides AL, John DR: Medullary sponge disease in horseshoe kidney. Urology 29: 426-427, 1987
-
(1987)
Urology
, vol.29
, pp. 426-427
-
-
Lambrianides, A.L.1
John, D.R.2
-
5
-
-
20844444776
-
An unusual association of contralateral congenital small kidney, reduced renal function and hyperparathyroidism in sponge kidney patients: On the track of the molecular basis
-
DOI 10.1093/ndt/gfh798
-
Gambaro G, Fabris A, Citron L, Tosetto E, Anglani F, Bellan F, Conte M, Bonfante L, Lupo A, D'Angelo A: An unusual association of contralateral congenital small kidney, reduced renal function and hyperparathyroidism in sponge kidney patients: On the track of the molecular basis. Nephrol Dial Transplant 20: 1042-1047, 2005 (Pubitemid 40862091)
-
(2005)
Nephrology Dialysis Transplantation
, vol.20
, pp. 1042-1047
-
-
Gambaro, G.1
Fabris, A.2
Citron, L.3
Tosetto, E.4
Anglani, F.5
Bellan, F.6
Conte, M.7
Bonfante, L.8
Lupo, A.9
D'Angelo, A.10
-
6
-
-
0014538730
-
Medullary sponge kidney with mega-pyelon and primary congenital megaureter in unilateral renal aplasia
-
Iwig J, Thiemann KJ: Medullary sponge kidney with mega-pyelon and primary congenital megaureter in unilateral renal aplasia. Fortschr Geb Rontgenstr Nuklearmed 111: 137-140, 1969
-
(1969)
Fortschr Geb Rontgenstr Nuklearmed
, vol.111
, pp. 137-140
-
-
Iwig, J.1
Thiemann, K.J.2
-
7
-
-
0014199860
-
Medullary sponge kidney: Its occurrence in a father and daughter
-
Copping GA: Medullary sponge kidney: Its occurrence in a father and daughter. CMAJ 96: 608-611, 1967
-
(1967)
CMAJ
, vol.96
, pp. 608-611
-
-
Copping, G.A.1
-
8
-
-
0015145774
-
Medullary sponge kidney in three generations
-
Kuiper JJ: Medullary sponge kidney in three generations. NY State J Med 71: 2665-2669, 1971
-
(1971)
NY State J Med
, vol.71
, pp. 2665-2669
-
-
Kuiper, J.J.1
-
9
-
-
32544439250
-
Medullary sponge kidney (Lenarduzzi-Cacchi-Ricci disease): A Padua Medical School discovery in the 1930s
-
DOI 10.1038/sj.ki.5000035, PII 5000035
-
Gambaro G, Feltrin GP, Lupo A, Bonfante L, D'Angelo A, Antonello A: Medullary sponge kidney (Lenarduzzi-Cacchi- Ricci disease): A Padua Medical School discovery in the 1930s. Kidney Int 69: 663-670, 2006 (Pubitemid 43237634)
-
(2006)
Kidney International
, vol.69
, Issue.4
, pp. 663-670
-
-
Gambaro, G.1
Feltrin, G.P.2
Lupo, A.3
Bonfante, L.4
D'Angelo, A.5
Antonello, A.6
-
10
-
-
0033658554
-
Association of medullary sponge kidney disease and multiple endocrine neoplasia type IIA due to RET gene mutation: Is there a causal relationship?
-
Diouf B, Ka EH, Calender A, Giraud S, Diop TM: Association of medullary sponge kidney disease and multiple endocrine neoplasia type IIA due to RET gene mutation: Is there a causal relationship?. Nephrol Dial Transplant 15: 2062-2066, 2000
-
(2000)
Nephrol Dial Transplant
, vol.15
, pp. 2062-2066
-
-
Diouf, B.1
Ka, E.H.2
Calender, A.3
Giraud, S.4
Diop, T.M.5
-
12
-
-
0033856620
-
Metanephrogenic mesenchyme-to epithelium transition induces profound expression changes of ion channels
-
Huber SM, Braun GS, Segerer S, Veh RW, Horster MF: Metanephrogenic mesenchyme-to epithelium transition induces profound expression changes of ion channels. Am J Renal Physiol 279: F65-F76, 2000
-
(2000)
Am J Renal Physiol
, vol.279
-
-
Huber, S.M.1
Braun, G.S.2
Segerer, S.3
Veh, R.W.4
Horster, M.F.5
-
13
-
-
0029901727
-
Renal agenesis and the absence of enteric neurons in mice lacking GDNF
-
DOI 10.1038/382070a0
-
Sánchez MP, Silos-Santiago I, Frisén J, He B, Lira SA, Barbacid M: Renal agenesis and the absence of enteric neurons in mice lacking GDNF. Nature 382: 70-73, 1996 (Pubitemid 26243359)
-
(1996)
Nature
, vol.382
, Issue.6586
, pp. 70-73
-
-
Sanchez, M.P.1
Silos-Santiago, I.2
Frisen, J.3
He, B.4
Lira, S.A.5
Barbacid, M.6
-
14
-
-
0028174023
-
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor RET
-
Schuchardt A, D'Agati V, Larsson-Blomberg L, Costantini F, Pachnis V: Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor RET. Nature 367: 380-383, 1994
-
(1994)
Nature
, vol.367
, pp. 380-383
-
-
Schuchardt, A.1
D'Agati, V.2
Larsson-Blomberg, L.3
Costantini, F.4
Pachnis, V.5
-
15
-
-
0035479144
-
The RET receptor: Function in development and dysfunction in congenital malformation
-
DOI 10.1016/S0168-9525(01)02420-9, PII S0168952501024209
-
Manie S, Santoro M, Fusco A, Billaud M: The RET receptor: Function in development and dysfunction in congenital malformation. Trends Genet 17: 580-589, 2001 (Pubitemid 32918300)
-
(2001)
Trends in Genetics
, vol.17
, Issue.10
, pp. 580-589
-
-
Manie, S.1
Santoro, M.2
Fusco, A.3
Billaud, M.4
-
16
-
-
40749161593
-
Renal aplasia in humans is associated with RET mutations
-
Skinner MA, Safford SD, Reeves JG, Jackson ME, Freemerman AJ: Renal aplasia in humans is associated with RET mutations. Am J Hum Genet 82: 344-351, 2008
-
(2008)
Am J Hum Genet
, vol.82
, pp. 344-351
-
-
Skinner, M.A.1
Safford, S.D.2
Reeves, J.G.3
Jackson, M.E.4
Freemerman, A.J.5
-
17
-
-
0034908554
-
Nomenclature for the description of human sequence variations
-
den Dunnen JT, Antonarakis SE: Nomenclature for the description of human sequence variations. Hum Genet 109: 121-124, 2001
-
(2001)
Hum Genet
, vol.109
, pp. 121-124
-
-
Den Dunnen, J.T.1
Antonarakis, S.E.2
-
18
-
-
0034743380
-
Quantitation of TGF-beta1 mRNA in porcine mesangial cells by comparative kinetic RT/PCR: Comparison with ribonuclease protection assay and in situ hybridization
-
Ceol M, Forino M, Gambaro G, Sauer U, Schleicher ED, D'Angelo A, Anglani F: Quantitation of TGF-beta1 mRNA in porcine mesangial cells by comparative kinetic RT/PCR: comparison with ribonuclease protection assay and in situ hybridization. J Clin Lab Anal 15: 215-222, 2001
-
(2001)
J Clin Lab Anal
, vol.15
, pp. 215-222
-
-
Ceol, M.1
Forino, M.2
Gambaro, G.3
Sauer, U.4
Schleicher, E.D.5
D'Angelo, A.6
Anglani, F.7
-
19
-
-
0028604499
-
GDNF is expressed in two forms in many tissues outside the CNS
-
Suter-Crazzolara C, Unsicker K: GDNF is expressed in two forms in many tissues outside the CNS. Neuroreport 5: 2486-2488, 1994
-
(1994)
Neuroreport
, vol.5
, pp. 2486-2488
-
-
Suter-Crazzolara, C.1
Unsicker, K.2
-
20
-
-
0034050323
-
Glial cell line-derived neurotrophic factor (GDNF) is expressed in the human kidney and is a growth factor for human mesangial cells
-
Orth SR, Ritz E, Suter-Crazzolara C: Glial cell line-derived neurotrophic factor (GDNF) is expressed in the human kidney and is a growth factor for human mesangial cells. Nephrol Dial Transplant 15: 589-595, 2000 (Pubitemid 30242974)
-
(2000)
Nephrology Dialysis Transplantation
, vol.15
, Issue.5
, pp. 589-595
-
-
Orth, S.R.1
Ritz, E.2
Suter-Crazzolara, C.3
-
21
-
-
0036896368
-
Glial cell line derived neurotrophic factor is expressed by the epithelia of human renal dysplasia
-
El-Ghoneimi A, Berrebi D, Levacher B, Nepote V, Infante M, Paris R, Simonneau M, Aigrain Y, Peuchmaur M: Glial cell line derived neurotrophic factor is expressed by epithelia of human renal dysplasia. J Urol 168: 2624-2628, 2002 (Pubitemid 35402704)
-
(2002)
Journal of Urology
, vol.168
, Issue.6
, pp. 2624-2628
-
-
El-Ghoneimi, A.1
Berrebi, D.2
Beatrice, L.3
Nepote, V.4
Hnfante, M.5
Paris, R.6
Simonneau, M.7
Aigrain, Y.8
Peuchmaur, M.9
-
22
-
-
0037103913
-
RET receptor tyrosine kinase isoforms in kidney function and disease
-
Lee DC, Chan KW, Chan SY: RET receptor tyrosine kinase isoforms in kidney function and disease. Oncogene 21: 5582-5592, 2002
-
(2002)
Oncogene
, vol.21
, pp. 5582-5592
-
-
Lee, D.C.1
Chan, K.W.2
Chan, S.Y.3
-
23
-
-
0035215311
-
Regulation of ureteric bud outgrowth by Pax2-dependent activation of the glial derived neurotrophic factor gene
-
Brophy PD, Ostrom L, Lang KM, Dressler GR: Regulation of ureteric bud outgrowth by Pax2-dependent activation of the glial derived neurotrophic factor gene. Development 128: 4747-4756, 2001 (Pubitemid 33138585)
-
(2001)
Development
, vol.128
, Issue.23
, pp. 4747-4756
-
-
Brophy, P.D.1
Ostrom, L.2
Lang, K.M.3
Dressler, G.R.4
-
24
-
-
67650283803
-
Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn
-
Zhang Z, Quinlan J, Grote D, Lemire M, Hudson T, Benjamin A, Roy A, Pascuet E, Goodyer M, Raju C, Houghton F, Bouchard M, Goodyer P: Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn. Pediatr Nephrol 24: 1151-1157, 2009
-
(2009)
Pediatr Nephrol
, vol.24
, pp. 1151-1157
-
-
Zhang, Z.1
Quinlan, J.2
Grote, D.3
Lemire, M.4
Hudson, T.5
Benjamin, A.6
Roy, A.7
Pascuet, E.8
Goodyer, M.9
Raju, C.10
Houghton, F.11
Bouchard, M.12
Goodyer, P.13
|