-
2
-
-
0033498215
-
Primary hyperoxaluria in infants: Medical, ethical, and economic issues
-
Cochat P, Koch Nogueira PC, Mahmoud MA, Jamieson NV, Scheinman JI, Rolland MO. Primary hyperoxaluria in infants: medical, ethical, and economic issues. J Pediatr 1999;135:746-749
-
(1999)
J Pediatr
, vol.135
, pp. 746-749
-
-
Cochat, P.1
Koch Nogueira, P.C.2
Mahmoud, M.A.3
Jamieson, N.V.4
Scheinman, J.I.5
Rolland, M.O.6
-
3
-
-
0031719134
-
A case of primary hyperoxaluria type 1 (PH-I) presented with black liver
-
Kazama-Saegua S, Kazama JJ, Sugaya U, Takamiya H, Terano A, Ichiyama A. A case of primary hyperoxaluria type 1 (PH-I) presented with black liver. Clin Nephrol 1998;50:184-187
-
(1998)
Clin Nephrol
, vol.50
, pp. 184-187
-
-
Kazama-Saegua, S.1
Kazama, J.J.2
Sugaya, U.3
Takamiya, H.4
Terano, A.5
Ichiyama, A.6
-
4
-
-
0035170499
-
Phenotypic expression of primary hyperoxaluria: Comparative features of type I and II
-
Milliner DS, Wilson DM, Smith LH. Phenotypic expression of primary hyperoxaluria: comparative features of type I and II. Kidney Internat 2001;59:31-36
-
(2001)
Kidney Internat
, vol.59
, pp. 31-36
-
-
Milliner, D.S.1
Wilson, D.M.2
Smith, L.H.3
-
5
-
-
0031979310
-
Variable presentation of primary hyperoxaluria type 1 in 2 patients homozygous for novel combined deletion and insertion mutation in exon 8 of the AGXT gene
-
von Schnakenburg C, Hulton SA, Milford DV, Roper HP, Rumsby G. Variable presentation of primary hyperoxaluria type 1 in 2 patients homozygous for novel combined deletion and insertion mutation in exon 8 of the AGXT gene. Nephron 1998;78:485-488
-
(1998)
Nephron
, vol.78
, pp. 485-488
-
-
Von Schnakenburg, C.1
Hulton, S.A.2
Milford, D.V.3
Roper, H.P.4
Rumsby, G.5
-
6
-
-
0033762190
-
Flexibility of melting temperature assay for rapid detection of insertions, deletions, and single-point mutations of the AGXT gene responsible for type 1 primary hyperoxaluria
-
Pirulli D, Boniotto M, Puzzer D, Spano A, Amoroso A, Crovella S. Flexibility of melting temperature assay for rapid detection of insertions, deletions, and single-point mutations of the AGXT gene responsible for type 1 primary hyperoxaluria. Clin Chem 2000;46:1842-1843
-
(2000)
Clin Chem
, vol.46
, pp. 1842-1843
-
-
Pirulli, D.1
Boniotto, M.2
Puzzer, D.3
Spano, A.4
Amoroso, A.5
Crovella, S.6
-
8
-
-
33747041816
-
What is new in primary hyperoxaluria?
-
Leumann E, Hoppe B. What is new in primary hyperoxaluria? Nephrol Dial Transplant 1995;16: 399-406
-
(1995)
Nephrol Dial Transplant
, vol.16
, pp. 399-406
-
-
Leumann, E.1
Hoppe, B.2
-
9
-
-
0030910117
-
Primary hyperoxaluria: Tunisian experience a propos of 24 pediatric cases
-
Kamoun A, Daudon M, Zghal A, et al. Primary hyperoxaluria: Tunisian experience a propos of 24 pediatric cases [in French]. Nephrologie 1997;18:59-64
-
(1997)
Nephrologie
, vol.18
, pp. 59-64
-
-
Kamoun, A.1
Daudon, M.2
Zghal, A.3
-
10
-
-
0033982863
-
Oxalosis with nephrocalcinosis
-
Singh DR, Sagade SN, Kamat MH, Deshpande RB, Shah BV. Oxalosis with nephrocalcinosis. Nephrol Dial Transplant 2000;15:124-125
-
(2000)
Nephrol Dial Transplant
, vol.15
, pp. 124-125
-
-
Singh, D.R.1
Sagade, S.N.2
Kamat, M.H.3
Deshpande, R.B.4
Shah, B.V.5
-
13
-
-
0025957665
-
Echogenic renal pyramids in children
-
Jequier S, Kaplan BS. Echogenic renal pyramids in children. J Clin Ultrasound 1991;19:85-92
-
(1991)
J Clin Ultrasound
, vol.19
, pp. 85-92
-
-
Jequier, S.1
Kaplan, B.S.2
|