-
1
-
-
0034093572
-
Hypomagnesaemia-hypercalciuria-nephrocalcinosis: A report of nine cases and a review
-
Benigno V., Canonica C.S., Bettinelli A. i wsp.: Hypomagnesaemia- hypercalciuria-nephrocalcinosis: A report of nine cases and a review. Nephrol. Dial. Transplant., 2000, 15, 605-610.
-
(2000)
Nephrol. Dial. Transplant.
, vol.15
, pp. 605-610
-
-
Benigno, V.1
Canonica, C.S.2
Bettinelli, A.3
-
2
-
-
0034999377
-
Paracellin-1 is critical for magnesium and calcium reabsorption in the human thick ascending limb of Henle
-
Blanchard A., Jeunemaitre X., Coudol P. i wsp.: Paracellin-1 is critical for magnesium and calcium reabsorption in the human thick ascending limb of Henle. Kidney Int., 2001, 59, 2206-2215.
-
(2001)
Kidney Int.
, vol.59
, pp. 2206-2215
-
-
Blanchard, A.1
Jeunemaitre, X.2
Coudol, P.3
-
3
-
-
0013976561
-
A New familial disorder characterized by hypokalemia and hypomagnezemia
-
Gitelman H.J., Graham J.B., Welt L.G.: A New familial disorder characterized by hypokalemia and hypomagnezemia. Trans. Assoc. Am. Physicians, 1966, 79, 221-233.
-
(1966)
Trans. Assoc. Am. Physicians
, vol.79
, pp. 221-233
-
-
Gitelman, H.J.1
Graham, J.B.2
Welt, L.G.3
-
4
-
-
3543141919
-
Hypomagnesemia associated with chemotherapy in patients treated for acute lymphoblastic leukemia: Possibile mechanisms
-
Guo C-Y., Halton J.M., Barr R.D. i wsp.: Hypomagnesemia associated with chemotherapy in patients treated for acute lymphoblastic leukemia: Possibile mechanisms. Oncol. Rep., 2004, 11, 185-189.
-
(2004)
Oncol. Rep.
, vol.11
, pp. 185-189
-
-
Guo, C.-Y.1
Halton, J.M.2
Barr, R.D.3
-
5
-
-
0026181318
-
Dietary fructose produces greater nephrocalcinosis in female than in male magnesium-deficient rats
-
Koh E.T., Min K.W.: Dietary fructose produces greater nephrocalcinosis in female than in male magnesium-deficient rats. Magnesium Res., 1991, 4, 97-103.
-
(1991)
Magnesium Res.
, vol.4
, pp. 97-103
-
-
Koh, E.T.1
Min, K.W.2
-
7
-
-
0036312673
-
Genetic disorders of magnesium homeostasis
-
Meji I.C., van den Heuvel L.P., Knoers N.V.: Genetic disorders of magnesium homeostasis. Biometals, 2002, 15, 297-307.
-
(2002)
Biometals
, vol.15
, pp. 297-307
-
-
Meji, I.C.1
Van Den Heuvel, L.P.2
Knoers, N.V.3
-
8
-
-
0015413157
-
Decreased bicarbonate threshold and renal magnesium casting in a sibship with distal renal tubular acidosis: Evaluation of the pathophysiological role of parathyroid hormone
-
Michelis M.F., Drash A.L., Linarelli L.G. i wsp.: Decreased bicarbonate threshold and renal magnesium casting in a sibship with distal renal tubular acidosis: Evaluation of the pathophysiological role of parathyroid hormone. Metabolism, 1972, 21, 905-920.
-
(1972)
Metabolism
, vol.21
, pp. 905-920
-
-
Michelis, M.F.1
Drash, A.L.2
Linarelli, L.G.3
-
9
-
-
0029020519
-
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis
-
Praga M., Vara J., Gonzalez-Parra E. i wsp.: Familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Kidney Int., 1995, 47, 1419-1425.
-
(1995)
Kidney Int.
, vol.47
, pp. 1419-1425
-
-
Praga, M.1
Vara, J.2
Gonzalez-Parra, E.3
-
10
-
-
0030707887
-
Renal magnesium handling: New insights in understanding old problems
-
Quamme G.A.: Renal magnesium handling: New insights in understanding old problems. Kidney Int., 1997, 52, 1180-1195.
-
(1997)
Kidney Int.
, vol.52
, pp. 1180-1195
-
-
Quamme, G.A.1
-
11
-
-
0342656513
-
Members of the Arbeitsgemeinschaft für pädiatrische Nephrologie: Nephrocalcinosis in children: A retrospective survey
-
Rönnefarth G., Misselwitz J.: Members of the Arbeitsgemeinschaft für pädiatrische Nephrologie: Nephrocalcinosis in children: a retrospective survey. Pediatr. Nephrol., 2000, 14, 1016-1021.
-
(2000)
Pediatr. Nephrol.
, vol.14
, pp. 1016-1021
-
-
Rönnefarth, G.1
Misselwitz, J.2
-
12
-
-
0346007915
-
Genetics of hereditary disorders of magnesium homeostasis
-
Schlingmann K.P., Konrad M., Seyberth H.W.: Genetics of hereditary disorders of magnesium homeostasis. Pediatr. Nephrol., 2004, 19, 13-25.
-
(2004)
Pediatr. Nephrol.
, vol.19
, pp. 13-25
-
-
Schlingmann, K.P.1
Konrad, M.2
Seyberth, H.W.3
-
14
-
-
0348161392
-
Two heterozygous mutations of CLDN 16 in a Japanese patient with FHHNC
-
Tajima T., Nakae J., Fujieda K.: Two heterozygous mutations of CLDN 16 in a Japanese patient with FHHNC. Pediatr. Nephrol., 2003, 18, 1280-1282.
-
(2003)
Pediatr. Nephrol.
, vol.18
, pp. 1280-1282
-
-
Tajima, T.1
Nakae, J.2
Fujieda, K.3
-
15
-
-
18244431922
-
Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PLCN-1 gene
-
Weber S., Hoffmann K., Jeck N. i wsp.: Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PLCN-1 gene. Eur. J. Hum. Genet., 2000, 8, 414-422.
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 414-422
-
-
Weber, S.1
Hoffmann, K.2
Jeck, N.3
-
16
-
-
0034863148
-
Novel Paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
-
Weber S., Schneider L., Peters M. i wsp.: Novel Paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. J. Am. Soc. Nephrol., 2001, 12, 1872-1881.
-
(2001)
J. Am. Soc. Nephrol.
, vol.12
, pp. 1872-1881
-
-
Weber, S.1
Schneider, L.2
Peters, M.3
-
17
-
-
0036956994
-
Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene
-
Wolf M.T.F., Dötsch J., Konrad M. i wsp.: Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene. Pediatr. Nephrol., 2002, 17, 602-608.
-
(2002)
Pediatr. Nephrol.
, vol.17
, pp. 602-608
-
-
Wolf, M.T.F.1
Dötsch, J.2
Konrad, M.3
-
18
-
-
0030053531
-
Hypermagnesiuria and hypercalciuria in childhood leukemia: An effect of amikacin therapy
-
Wu B., Atkinson S.A., Halton J.M. i wsp.: Hypermagnesiuria and hypercalciuria in childhood leukemia: an effect of amikacin therapy. J. Pediatr. Hematol. Oncol., 1996, 18, 86-89.
-
(1996)
J. Pediatr. Hematol. Oncol.
, vol.18
, pp. 86-89
-
-
Wu, B.1
Atkinson, S.A.2
Halton, J.M.3
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