-
1
-
-
0025820451
-
Familial hypomagnesemia with secondary hypocalcemia. Autosomal or X-linked inheritance?
-
Pronicka E, Gruszczynska B. Familial hypomagnesemia with secondary hypocalcemia. Autosomal or X-linked inheritance? J Inher Metab Dis 1991;14:397-9.
-
(1991)
J Inher Metab Dis
, vol.14
, pp. 397-399
-
-
Pronicka, E.1
Gruszczynska, B.2
-
2
-
-
0018645514
-
Studies in primary hypomagnesemia: Evidence for defective carrier-mediated small intestinal transport of magnesium
-
Milla P, Agget PJ, Wolff OH, et al. Studies in primary hypomagnesemia: Evidence for defective carrier-mediated small intestinal transport of magnesium. Gut 1979;20:1028-33.
-
(1979)
Gut
, vol.20
, pp. 1028-1033
-
-
Milla, P.1
Agget, P.J.2
Wolff, O.H.3
-
3
-
-
0014249537
-
Primary hypomagnesemia with secondary hypocalcemia in an infant
-
Paunier LRadde IC, Kooh SW, et al. Primary hypomagnesemia with secondary hypocalcemia in an infant. Pediatrics 1968;41:385-402.
-
(1968)
Pediatrics
, vol.41
, pp. 385-402
-
-
Paunier, L.1
Radde, I.C.2
Kooh, S.W.3
-
4
-
-
84920233510
-
Primary hypomagnesemia, an X-borne allele?
-
Teebi AS. Primary hypomagnesemia, an X-borne allele? Lancet 1983; 1:701.
-
(1983)
Lancet
, vol.1
, pp. 701
-
-
Teebi, A.S.1
-
5
-
-
0028183151
-
Hypomagnesemia with secondary hypocalcemia in a female with a balance X:9 translocation: Mapping of the Xp22 chromosome breakpoint
-
Chery M, Biancalana V, Philippe C, et al. Hypomagnesemia with secondary hypocalcemia in a female with a balance X:9 translocation: Mapping of the Xp22 chromosome breakpoint. Hum Genet 1994;93:587-91.
-
(1994)
Hum Genet
, vol.93
, pp. 587-591
-
-
Chery, M.1
Biancalana, V.2
Philippe, C.3
-
6
-
-
0019492106
-
Familial hypomagnesemia: A follow-up examination of three patients after 9 to 12 years of treatment
-
Stramme JH, Steen-Johnsen J, Hamaes K, et al. Familial hypomagnesemia: A follow-up examination of three patients after 9 to 12 years of treatment. Pediatr Res 1981;15:1134-9.
-
(1981)
Pediatr Res
, vol.15
, pp. 1134-1139
-
-
Stramme, J.H.1
Steen-Johnsen, J.2
Hamaes, K.3
-
7
-
-
0024496661
-
Primary infantile hypomagnesaemia: Report of two cases and review of literature
-
Adulrazzaq YM, Smigura FC, Wettrell G. Primary infantile hypomagnesaemia: Report of two cases and review of literature. Eur J Pediatr 1989;148:459-61.
-
(1989)
Eur J Pediatr
, vol.148
, pp. 459-461
-
-
Adulrazzaq, Y.M.1
Smigura, F.C.2
Wettrell, G.3
-
8
-
-
0015515015
-
Evidence for parathyroid failure in magnesium deficiency
-
Anast CS, Mohs JM, Kaplan SL, et al. Evidence for parathyroid failure in magnesium deficiency. Science 1972;177:606-8.
-
(1972)
Science
, vol.177
, pp. 606-608
-
-
Anast, C.S.1
Mohs, J.M.2
Kaplan, S.L.3
-
9
-
-
0015951179
-
Idiopathic hypomagnesemia with hypocalcemia in an adult
-
Coenegractit JM, Houben HGJ. Idiopathic hypomagnesemia with hypocalcemia in an adult. Clin Chim Acta 1974;50:349-57.
-
(1974)
Clin Chim Acta
, vol.50
, pp. 349-357
-
-
Coenegractit, J.M.1
Houben, H.G.J.2
-
12
-
-
0021781136
-
Parenteral magnesium tolerance testing in the evaluation of magnesium deficiency
-
Ryzen E, Elbaum N, Singer FR, et al. Parenteral magnesium tolerance testing in the evaluation of magnesium deficiency. Magnesium 1985; 4:137-47.
-
(1985)
Magnesium
, vol.4
, pp. 137-147
-
-
Ryzen, E.1
Elbaum, N.2
Singer, F.R.3
|