-
1
-
-
0041630593
-
Chronic renal insufficiency in children: The 2001 annual report of the NAPRTCS
-
Seikaly MG, Ho PL, Emmett L, Fine RN, Tejani A. Chronic renal insufficiency in children: the 2001 annual report of the NAPRTCS. Pediatr Nephrol 2003;18:796-804.
-
(2003)
Pediatr Nephrol
, vol.18
, pp. 796-804
-
-
Seikaly, M.G.1
Ho, P.L.2
Emmett, L.3
Fine, R.N.4
Tejani, A.5
-
2
-
-
0033781313
-
The EPICure study: Outcomes to discharge from hospital for infants born at the threshold of viability
-
Costeloe K, Hennessy E, Gibson AT, Marlow N, Wilkinson AR. The EPICure study: outcomes to discharge from hospital for infants born at the threshold of viability. Pediatrics 2000;106:659-671.
-
(2000)
Pediatrics
, vol.106
, pp. 659-671
-
-
Costeloe, K.1
Hennessy, E.2
Gibson, A.T.3
Marlow, N.4
Wilkinson, A.R.5
-
3
-
-
0029036339
-
Effects of ureteral obstruction on renal growth
-
Chevalier RL. Effects of ureteral obstruction on renal growth. Semin Nephrol 1995;15:353-360.
-
(1995)
Semin Nephrol
, vol.15
, pp. 353-360
-
-
Chevalier, R.L.1
-
4
-
-
0001934046
-
Urogenital system
-
Baltimore: Williams & Wilkins
-
Sadler TW. Urogenital system. In eds. Langman's Medical Embryology. Baltimore: Williams & Wilkins, 1990, p.260.
-
(1990)
Langman's Medical Embryology
, pp. 260
-
-
Sadler, T.W.1
-
5
-
-
2342418469
-
Branching morphogenesis and kidney disease
-
Shah MM, Sampogna V, Sakurai H, Bush KT, Nigam SK. Branching morphogenesis and kidney disease. Development 2004;131:1443-1462.
-
(2004)
Development
, vol.131
, pp. 1443-1462
-
-
Shah, M.M.1
Sampogna, V.2
Sakurai, H.3
Bush, K.T.4
Nigam, S.K.5
-
6
-
-
0028307612
-
Pharmacology of antineoplastic agents in pregnancy
-
Wiebe VJ, Sipila PE. Pharmacology of antineoplastic agents in pregnancy. Crit Rev Oncol Hematol 1994;16:75-112.
-
(1994)
Crit Rev Oncol Hematol
, vol.16
, pp. 75-112
-
-
Wiebe, V.J.1
Sipila, P.E.2
-
7
-
-
84872623412
-
Facial characteristics of infants with bilateral renal agenesis
-
Potter EL. Facial characteristics of infants with bilateral renal agenesis. Am J Obstet Gynecol 1946;41:885-888.
-
(1946)
Am J Obstet Gynecol
, vol.41
, pp. 885-888
-
-
Potter, E.L.1
-
10
-
-
0027182741
-
WT-1 is required for early kidney development
-
Kreidberg JA, Sariola H, Loring JM, Maeda M, Pelletier J, Housman D, Jaenisch R. WT-1 is required for early kidney development. Cell 1993;74:679-691.
-
(1993)
Cell
, vol.74
, pp. 679-691
-
-
Kreidberg, J.A.1
Sariola, H.2
Loring, J.M.3
Maeda, M.4
Pelletier, J.5
Housman, D.6
Jaenisch, R.7
-
11
-
-
0019362340
-
The pathogenesis of renal dysplasia II. The significance of lateral and medial ectopy of the ureteric orifice
-
Schwarz RD, Stephens FD, Gussen LJ. The pathogenesis of renal dysplasia II. The significance of lateral and medial ectopy of the ureteric orifice. Invest Urol 1981;19:97-100.
-
(1981)
Invest Urol
, vol.19
, pp. 97-100
-
-
Schwarz, R.D.1
Stephens, F.D.2
Gussen, L.J.3
-
12
-
-
0015609511
-
Position and configuration of the ureteral orifice and its relationship to renal scarring in adults
-
Vermillion CD, Heale WF. Position and configuration of the ureteral orifice and its relationship to renal scarring in adults. J Urol 1973;109:579-584.
-
(1973)
J Urol
, vol.109
, pp. 579-584
-
-
Vermillion, C.D.1
Heale, W.F.2
-
13
-
-
0033694018
-
Potential biological role of transforming growth factor-β1 in human congenital kidney malformations
-
Yang SP, Woolf AS, Yuan HT, Scott RJ, Risdon RA, O'Hare MJ, Winyard PJ. Potential biological role of transforming growth factor-β1 in human congenital kidney malformations. Am J Pathol 2000;157:1633-1647.
-
(2000)
Am J Pathol
, vol.157
, pp. 1633-1647
-
-
Yang, S.P.1
Woolf, A.S.2
Yuan, H.T.3
Scott, R.J.4
Risdon, R.A.5
O'Hare, M.J.6
Winyard, P.J.7
-
14
-
-
0027756731
-
A quantitative study of normal nephrogenesis in the human fetus: Its implications in the natural history of kidney changes due to low obstructive uropathies
-
Gasser B, Mauss Y, Ghnassia JP, Kohler M, Yu O, Vonesch JL. A quantitative study of normal nephrogenesis in the human fetus: its implications in the natural history of kidney changes due to low obstructive uropathies. Fetal Diagn Ther 1993;8:371-384.
-
(1993)
Fetal Diagn Ther
, vol.8
, pp. 371-384
-
-
Gasser, B.1
Mauss, Y.2
Ghnassia, J.P.3
Kohler, M.4
Yu, O.5
Vonesch, J.L.6
-
15
-
-
1642504431
-
A functional immature model of chronic partial ureteral obstruction
-
Beharrie A, Franc-Guimond J, Rodriguez MM, Au J, Zilleruelo G, Abitbol CL. A functional immature model of chronic partial ureteral obstruction. Kidney Int 2004;65:1155-1161.
-
(2004)
Kidney Int
, vol.65
, pp. 1155-1161
-
-
Beharrie, A.1
Franc-Guimond, J.2
Rodriguez, M.M.3
Au, J.4
Zilleruelo, G.5
Abitbol, C.L.6
-
16
-
-
0043131813
-
Prenatal ultrasound guided percutaneous shunts for obstructive uropathy and thoracic disease
-
Wilson RD, Johnson MP. Prenatal ultrasound guided percutaneous shunts for obstructive uropathy and thoracic disease. Semin Pediatr Surg 2003;12:182-189.
-
(2003)
Semin Pediatr Surg
, vol.12
, pp. 182-189
-
-
Wilson, R.D.1
Johnson, M.P.2
-
17
-
-
0015801948
-
Familial bilateral renal agenesis and hereditary renal adysplasia
-
Buchta RM, Viseskul C, Gilbert EF, Sarto GE, Opitz JM. Familial bilateral renal agenesis and hereditary renal adysplasia. Z Kinderheilkd 1973;115:111-129.
-
(1973)
Z Kinderheilkd
, vol.115
, pp. 111-129
-
-
Buchta, R.M.1
Viseskul, C.2
Gilbert, E.F.3
Sarto, G.E.4
Opitz, J.M.5
-
18
-
-
0028260260
-
Hereditary renal adysplasia: New observations and hypotheses
-
Moerman P, Fryns JP, Sastrowijoto SH, Vandenberghe K, Lauweryns JM. Hereditary renal adysplasia: new observations and hypotheses. Pediatr Pathol 1994;4:405-410.
-
(1994)
Pediatr Pathol
, vol.4
, pp. 405-410
-
-
Moerman, P.1
Fryns, J.P.2
Sastrowijoto, S.H.3
Vandenberghe, K.4
Lauweryns, J.M.5
-
19
-
-
0021339670
-
Familial nature of congenital absence and severe dysgenesis of both kidneys
-
Roodhoof AM, Birnholtz JC, Holmes LB. Familial nature of congenital absence and severe dysgenesis of both kidneys. N Engl J Med 1984;310:1341-1345.
-
(1984)
N Engl J Med
, vol.310
, pp. 1341-1345
-
-
Roodhoof, A.M.1
Birnholtz, J.C.2
Holmes, L.B.3
-
20
-
-
12644280361
-
Unilateral hereditary hydronephrosis: A report of four cases in three consecutive generations
-
Jewell JH, Buchert WI. Unilateral hereditary hydronephrosis: a report of four cases in three consecutive generations. J Urol 1962;88:129-136.
-
(1962)
J Urol
, vol.88
, pp. 129-136
-
-
Jewell, J.H.1
Buchert, W.I.2
-
21
-
-
0026744209
-
Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p
-
Izquierdo L, Porteous M, Paramo PG, Conner JM. Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p. Hum Genet 1992;89:557-560.
-
(1992)
Hum Genet
, vol.89
, pp. 557-560
-
-
Izquierdo, L.1
Porteous, M.2
Paramo, P.G.3
Conner, J.M.4
-
22
-
-
0030447827
-
Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasia
-
Groener PM, Garcia E, Debeer P, Devriendt K, Fryns JP, Van de Ven WJ. Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasia. Genomics 1996;38:141-148.
-
(1996)
Genomics
, vol.38
, pp. 141-148
-
-
Groener, P.M.1
Garcia, E.2
Debeer, P.3
Devriendt, K.4
Fryns, J.P.5
Van De Ven, W.J.6
-
23
-
-
0026455194
-
The transmission of vesico-ureteral reflux from parent to child
-
Noe HN, Wyatt RJ, Peeden JN, Rivas ML. The transmission of vesico-ureteral reflux from parent to child. J Urol 1992;148:1869-1871.
-
(1992)
J Urol
, vol.148
, pp. 1869-1871
-
-
Noe, H.N.1
Wyatt, R.J.2
Peeden, J.N.3
Rivas, M.L.4
-
24
-
-
0036837263
-
Screening siblings for vesico-ureteral reflux
-
Hollowell JG, Greenfield SP. Screening siblings for vesico-ureteral reflux. J Urol 2002;168:2138-2141.
-
(2002)
J Urol
, vol.168
, pp. 2138-2141
-
-
Hollowell, J.G.1
Greenfield, S.P.2
-
25
-
-
0033910650
-
Primary nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1
-
Feather SA, Malcolm S, Woolf AS, Wright V, Blaydon D, Reid CJ, et al. Primary nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1. Am J Hum Genet 2000;66:1420-1425.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1420-1425
-
-
Feather, S.A.1
Malcolm, S.2
Woolf, A.S.3
Wright, V.4
Blaydon, D.5
Reid, C.J.6
-
26
-
-
0021280772
-
The Meckel syndrome: Clinicopathological findings in 67 patients
-
Salonen R. The Meckel syndrome: clinicopathological findings in 67 patients. Am J Med Genet 1984;18:671-689.
-
(1984)
Am J Med Genet
, vol.18
, pp. 671-689
-
-
Salonen, R.1
-
27
-
-
0019120132
-
Short rib polydactyly syndrome, Majewski type
-
Chen H, Yang SS, Gonzalez E, Fowler M, Al Saadi A. Short rib polydactyly syndrome, Majewski type. Am J Med Genet 1980;7:215-222.
-
(1980)
Am J Med Genet
, vol.7
, pp. 215-222
-
-
Chen, H.1
Yang, S.S.2
Gonzalez, E.3
Fowler, M.4
Al Saadi, A.5
-
28
-
-
0027225492
-
New findings in short rib syndrome
-
Cideciyan D, Rodriguez MM, Haun RL, Abdenour GE, Bruce JH. New findings in short rib syndrome. Am J Med Genet 1993;46:255-259.
-
(1993)
Am J Med Genet
, vol.46
, pp. 255-259
-
-
Cideciyan, D.1
Rodriguez, M.M.2
Haun, R.L.3
Abdenour, G.E.4
Bruce, J.H.5
-
29
-
-
0033615563
-
Recurrent cerebral infarctions and del(10)(p14p15.1) de novo in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome
-
Fujimoto S, Yokochi K, Morikawa H, Nakano M, Shibata H, Togari H, Wada Y. Recurrent cerebral infarctions and del(10)(p14p15.1) de novo in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome. Am J Med Genet 1999;86:427-429.
-
(1999)
Am J Med Genet
, vol.86
, pp. 427-429
-
-
Fujimoto, S.1
Yokochi, K.2
Morikawa, H.3
Nakano, M.4
Shibata, H.5
Togari, H.6
Wada, Y.7
-
30
-
-
0026728345
-
Brief report: Autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia
-
Bilous RW, Murty G, Parkinson DB, Thakker RV, Coulthard MG, Burn J, et al. Brief report: autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia. N Engl J Med 1992;327:1069-1074.
-
(1992)
N Engl J Med
, vol.327
, pp. 1069-1074
-
-
Bilous, R.W.1
Murty, G.2
Parkinson, D.B.3
Thakker, R.V.4
Coulthard, M.G.5
Burn, J.6
-
31
-
-
0025951601
-
Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay
-
Shaw NJ, Haigh D, Lealmann GT, Karbani G, Brocklebank JT, Dillon MJ. Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay. Arch Dis Child 1991;66:1191-1194.
-
(1991)
Arch Dis Child
, vol.66
, pp. 1191-1194
-
-
Shaw, N.J.1
Haigh, D.2
Lealmann, G.T.3
Karbani, G.4
Brocklebank, J.T.5
Dillon, M.J.6
-
32
-
-
50549169392
-
Multiple congenital anomaly caused by an extra autosome
-
Patau K, Smith DW, Therman E, Inhorn SL, Wagner HP. Multiple congenital anomaly caused by an extra autosome. Lancet 1960;275:790-793.
-
(1960)
Lancet
, vol.275
, pp. 790-793
-
-
Patau, K.1
Smith, D.W.2
Therman, E.3
Inhorn, S.L.4
Wagner, H.P.5
-
33
-
-
0024215591
-
The pathology of trisomy 13. A study of 12 cases
-
Moerman P, Fryns, van der Steen K, Kleczkowska A, Lauweryns J. The pathology of trisomy 13. A study of 12 cases. Hum Genet 1988;80:349-356.
-
(1988)
Hum Genet
, vol.80
, pp. 349-356
-
-
Moerman, P.1
Fryns2
Van Der Steen, K.3
Kleczkowska, A.4
Lauweryns, J.5
-
34
-
-
0015848845
-
Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome
-
Goldfischer S, Moore CL, Johnson AB, Spiro AJ, Valsamis MP, Wisniewski HK, et al. Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome. Science 1973;182:62-64.
-
(1973)
Science
, vol.182
, pp. 62-64
-
-
Goldfischer, S.1
Moore, C.L.2
Johnson, A.B.3
Spiro, A.J.4
Valsamis, M.P.5
Wisniewski, H.K.6
-
35
-
-
0021347101
-
New syndrome: Renal dysplasia, mesomelia, and radiohumeral fusion
-
Ulbright CE, Hodes ME, Ulbright TM. New syndrome: renal dysplasia, mesomelia, and radiohumeral fusion. Am J Med Genet 1984;17:667-668.
-
(1984)
Am J Med Genet
, vol.17
, pp. 667-668
-
-
Ulbright, C.E.1
Hodes, M.E.2
Ulbright, T.M.3
-
36
-
-
0025025724
-
Limb reduction defects and renal dysplasia: Confirmation of a new, apparently lethal, autosomal recessive MCA syndrome
-
Schrander-Stumpel C, de Die-Smulders C, Fryns JP, da Costa J, Bouckaert P. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome. Am J Med Genet 1990;37:133-135.
-
(1990)
Am J Med Genet
, vol.37
, pp. 133-135
-
-
Schrander-Stumpel, C.1
De Die-Smulders, C.2
Fryns, J.P.3
Da Costa, J.4
Bouckaert, P.5
-
37
-
-
0016716678
-
Autosomal dominant branchiootorenal dysplasia
-
Melnick M, Bixler D, Silk K, Yune H, Nance WE. Autosomal dominant branchiootorenal dysplasia. Birth Defects Original Article Series XI 1975;(5):121.
-
(1975)
Birth Defects Original Article Series XI
, Issue.5
, pp. 121
-
-
Melnick, M.1
Bixler, D.2
Silk, K.3
Yune, H.4
Nance, W.E.5
-
38
-
-
0032513573
-
Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13
-
Kumar S, Marres HA, Cor WR, Cremers CW, Kimberling WJ. Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13. Am J Med Genet 1998;76:395-401.
-
(1998)
Am J Med Genet
, vol.76
, pp. 395-401
-
-
Kumar, S.1
Marres, H.A.2
Cor, W.R.3
Cremers, C.W.4
Kimberling, W.J.5
-
39
-
-
0033942027
-
Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: Clinical and genetic implications
-
Kumar S, Deffenbacher K, Marres HA, Cor WR, Cremers CW, Kimberling WJ. Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications. Am J Hum Genet 2000;66:1715-1720.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1715-1720
-
-
Kumar, S.1
Deffenbacher, K.2
Marres, H.A.3
Cor, W.R.4
Cremers, C.W.5
Kimberling, W.J.6
-
40
-
-
0028304849
-
Caudal regression syndrome: Etiopathogenesis, prenatal diagnosis, and perinatal management
-
Adra A, Cordero D, Mejides A, Yasin S, Salman F, O'Sullivan MJ. Caudal regression syndrome: etiopathogenesis, prenatal diagnosis, and perinatal management. Obstet Gynecol Surv 1994;49:508-516.
-
(1994)
Obstet Gynecol Surv
, vol.49
, pp. 508-516
-
-
Adra, A.1
Cordero, D.2
Mejides, A.3
Yasin, S.4
Salman, F.5
O'Sullivan, M.J.6
-
41
-
-
0035180570
-
Embryonic gut anomalies in a mouse model of retinoic acid-induced caudal regression syndrome
-
Pitera JE, Smith VV, Wolf AS, Milla PJ. Embryonic gut anomalies in a mouse model of retinoic acid-induced caudal regression syndrome. Am J Pathol 2001;159:2321-2329.
-
(2001)
Am J Pathol
, vol.159
, pp. 2321-2329
-
-
Pitera, J.E.1
Smith, V.V.2
Wolf, A.S.3
Milla, P.J.4
-
42
-
-
0036788475
-
Sonographic diagnosis of caudal regression in the first trimester of pregnancy
-
Gonzalez-Quintero VH, Tolaymat L, Martin D, Romaguera RL, Rodríguez MM, Izquierdo LA. Sonographic diagnosis of caudal regression in the first trimester of pregnancy. J Ultrasound Med 2002;21:1175-1178.
-
(2002)
J Ultrasound Med
, vol.21
, pp. 1175-1178
-
-
Gonzalez-Quintero, V.H.1
Tolaymat, L.2
Martin, D.3
Romaguera, R.L.4
Rodríguez, M.M.5
Izquierdo, L.A.6
-
43
-
-
0346335999
-
Renal development in high-glucose ambience and diabetic embryopathy
-
Chugh SS, Wallner EI, Kanwar YS. Renal development in high-glucose ambience and diabetic embryopathy. Semin Nephrol 2003;23:583-592.
-
(2003)
Semin Nephrol
, vol.23
, pp. 583-592
-
-
Chugh, S.S.1
Wallner, E.I.2
Kanwar, Y.S.3
-
44
-
-
0024592194
-
Evidence of multifactorial origin of diabetes-induced embryopathies
-
Sadler TW, Hunter ES, Wynn RE, Phillips LS. Evidence of multifactorial origin of diabetes-induced embryopathies. Diabetes 1989;38:70-74.
-
(1989)
Diabetes
, vol.38
, pp. 70-74
-
-
Sadler, T.W.1
Hunter, E.S.2
Wynn, R.E.3
Phillips, L.S.4
-
45
-
-
0033857531
-
The missing link: A single unifying mechanism for diabetic complications
-
Nishikawa T, Edelstein D, Brownlee M. The missing link: a single unifying mechanism for diabetic complications. Kidney Int Suppl 2000;77:S26-S30.
-
(2000)
Kidney Int Suppl
, vol.77
-
-
Nishikawa, T.1
Edelstein, D.2
Brownlee, M.3
-
46
-
-
0036724696
-
Diacylglycerol production and protein kinase C activity are increased in a mouse model of diabetic embryopathy
-
Hiramatsu Y, Sekiguchi N, Hayashi M, Issihiki K, Yokota T, King GL, Loeken MR. Diacylglycerol production and protein kinase C activity are increased in a mouse model of diabetic embryopathy. Diabetes 2002;51:2804-2810.
-
(2002)
Diabetes
, vol.51
, pp. 2804-2810
-
-
Hiramatsu, Y.1
Sekiguchi, N.2
Hayashi, M.3
Issihiki, K.4
Yokota, T.5
King, G.L.6
Loeken, M.R.7
-
47
-
-
0023940456
-
Variable expression of autosomal recessive polycystic kidney disease and congenital hepatic fibrosis within a family
-
Kaplan BS, Kaplan P, de Chadarevian JP, Jequier S, O'Regan S, Russo P. Variable expression of autosomal recessive polycystic kidney disease and congenital hepatic fibrosis within a family. Am J Med Genet 1988;29:639-647.
-
(1988)
Am J Med Genet
, vol.29
, pp. 639-647
-
-
Kaplan, B.S.1
Kaplan, P.2
De Chadarevian, J.P.3
Jequier, S.4
O'Regan, S.5
Russo, P.6
-
48
-
-
0036509712
-
The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein
-
Ward CJ, Hogan MC, Rossetti S, Walker D, Sneddon T, Wang X, et al. The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein. Nat Genet 2002;30:259-269.
-
(2002)
Nat Genet
, vol.30
, pp. 259-269
-
-
Ward, C.J.1
Hogan, M.C.2
Rossetti, S.3
Walker, D.4
Sneddon, T.5
Wang, X.6
-
49
-
-
0345304730
-
Molecular genetics of autosomal dominant polycystic kidney disease
-
Pei Y. Molecular genetics of autosomal dominant polycystic kidney disease. Clin Invest Med, 2003;26:252-258.
-
(2003)
Clin Invest Med
, vol.26
, pp. 252-258
-
-
Pei, Y.1
-
50
-
-
0034214837
-
Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant gene, PKD1
-
2999
-
Ibraghimov-Beskrovnaya O, Bukanov NO, Donohue LC, Dackowski WR, Klinger KW, Landes GM. Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant gene, PKD1. Hum Molec Genet 2999;9:1641-1649.
-
Hum Molec Genet
, vol.9
, pp. 1641-1649
-
-
Ibraghimov-Beskrovnaya, O.1
Bukanov, N.O.2
Donohue, L.C.3
Dackowski, W.R.4
Klinger, K.W.5
Landes, G.M.6
-
51
-
-
0028030817
-
Incidence of renal anomalies in children prenatally exposed to ethanol
-
Taylor CL, Jones KL, Jones MC, Kaplan GW. Incidence of renal anomalies in children prenatally exposed to ethanol. Pediatrics 1994;94:209-212.
-
(1994)
Pediatrics
, vol.94
, pp. 209-212
-
-
Taylor, C.L.1
Jones, K.L.2
Jones, M.C.3
Kaplan, G.W.4
-
52
-
-
0025875281
-
Pathogenesis of ethanol-induced hydronephrosis and hydroureter as demonstrated following in vivo exposure of mouse embryos
-
Gage JC, Sulick KK. Pathogenesis of ethanol-induced hydronephrosis and hydroureter as demonstrated following in vivo exposure of mouse embryos. Teratology 1991;44:299-312.
-
(1991)
Teratology
, vol.44
, pp. 299-312
-
-
Gage, J.C.1
Sulick, K.K.2
-
53
-
-
0035862977
-
The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures
-
Abu-Abed S, Dolle P, Metzger D, Beckett B, Chambon P, Petkovich M. The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures. Genes Dev 2001;15:226-240.
-
(2001)
Genes Dev
, vol.15
, pp. 226-240
-
-
Abu-Abed, S.1
Dolle, P.2
Metzger, D.3
Beckett, B.4
Chambon, P.5
Petkovich, M.6
-
54
-
-
1942534671
-
Histomorphometric analysis of postnatal glomerulogenesis in extremely preterm infants
-
Rodriguez MM, Gómez AH, Abitbol CL, Chandar JJ, Duara S, Zilleruelo GE. Histomorphometric analysis of postnatal glomerulogenesis in extremely preterm infants. Pediatr Dev Pathol 2004;7:17-25.
-
(2004)
Pediatr Dev Pathol
, vol.7
, pp. 17-25
-
-
Rodriguez, M.M.1
Gómez, A.H.2
Abitbol, C.L.3
Chandar, J.J.4
Duara, S.5
Zilleruelo, G.E.6
-
55
-
-
0042030805
-
Investigating the newborn kidney: Update on imagin technique
-
Gordon I, Riccabona M. Investigating the newborn kidney: update on imagin technique. Semin Neonatol 2003;8:269-278.
-
(2003)
Semin Neonatol
, vol.8
, pp. 269-278
-
-
Gordon, I.1
Riccabona, M.2
-
56
-
-
8344272186
-
Is there significant improvement in neonatal outcome after treating pPROM mothers with ammo-infusion?
-
De Carolis MP, Romagnoli C, de Santis M, Piersigilli F, Vento G, Caruso A. Is there significant improvement in neonatal outcome after treating pPROM mothers with ammo-infusion? Biol Neonate 2004;8:222-229.
-
(2004)
Biol Neonate
, vol.8
, pp. 222-229
-
-
De Carolis, M.P.1
Romagnoli, C.2
De Santis, M.3
Piersigilli, F.4
Vento, G.5
Caruso, A.6
-
57
-
-
0042697656
-
Prenatal bladder drainage in the management of fetal lower urinary tract obstruction: A systematic review and meta-analysis
-
Clark TJ, Martin WL, Divakaran TG, Whittle MJ, Kilby MD, Khan KS. Prenatal bladder drainage in the management of fetal lower urinary tract obstruction: a systematic review and meta-analysis. Obstet Gynecol 2003;102:367-382.
-
(2003)
Obstet Gynecol
, vol.102
, pp. 367-382
-
-
Clark, T.J.1
Martin, W.L.2
Divakaran, T.G.3
Whittle, M.J.4
Kilby, M.D.5
Khan, K.S.6
-
58
-
-
0025879424
-
Complementary DNA sequencing: "expressed sequence tags" and the Human Genome Project
-
Adams MD, Kelley JM, Gocayne JD, Dubnick M, Polymeropoulus MH, Xiao H, Merril CR, Wu A, Olde B, et al. Complementary DNA sequencing: "expressed sequence tags" and the Human Genome Project. Science 1991;252:1651-1656.
-
(1991)
Science
, vol.252
, pp. 1651-1656
-
-
Adams, M.D.1
Kelley, J.M.2
Gocayne, J.D.3
Dubnick, M.4
Polymeropoulus, M.H.5
Xiao, H.6
Merril, C.R.7
Wu, A.8
Olde, B.9
-
59
-
-
0033958504
-
Future molecular approaches to the diagnosis and treatment of glomerular disease
-
Alcorta DA, Prakash K, Waga I, Sasai H, Munger W, Jeannette JC, Falk RJ. Future molecular approaches to the diagnosis and treatment of glomerular disease. Semin Nephrol 2000:20-31.
-
(2000)
Semin Nephrol
, pp. 20-31
-
-
Alcorta, D.A.1
Prakash, K.2
Waga, I.3
Sasai, H.4
Munger, W.5
Jeannette, J.C.6
Falk, R.J.7
-
61
-
-
0030733083
-
Glial-cell-line derived neurotrophic factor is required for bud initiation from ureteric epithelium
-
Saino K, Suvanto P, Davies J, Wartiovaara J, Wartiovaara K, Saarma M, et al. Glial-cell-line derived neurotrophic factor is required for bud initiation from ureteric epithelium. Development 1997;124:407-487.
-
(1997)
Development
, vol.124
, pp. 407-487
-
-
Saino, K.1
Suvanto, P.2
Davies, J.3
Wartiovaara, J.4
Wartiovaara, K.5
Saarma, M.6
|