A Loss-of-Function Mutation in NaPi-IIa and Renal Fanconi's Syndrome
Magen, Daniella, Berger, Liron, Coady, Michael J, Ilivitzki, Anat, Militianu, Daniela, Tieder, Martin, Selig, Sara, Lapointe, Jean Yves, Zelikovic, Israel, Skorecki, Karl
Published in The New England journal of medicine (25.03.2010)
Published in The New England journal of medicine (25.03.2010)
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Journal Article
SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis
Bergwitz, Clemens, Roslin, Nicole M, Tieder, Martin, Loredo-Osti, J C, Bastepe, Murat, Abu-Zahra, Hilal, Frappier, Danielle, Burkett, Kelly, Carpenter, Thomas O, Anderson, Donald, Garabedian, Michele, Sermet, Isabelle, Fujiwara, T Mary, Morgan, Kenneth, Tenenhouse, Harriet S, Juppner, Harald
Published in American journal of human genetics (01.02.2006)
Published in American journal of human genetics (01.02.2006)
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Journal Article
Idiopathic Hypercalciuria and Hereditary Hypophosphatemic Rickets
Tieder, Martin, Modai, David, Shared, Uri, Samuel, Ruth, Arie, Raphael, Halabe, Aharon, Maor, Joseph, Weissgarten, Joshua, Averbukh, Zhan, Cohen, Natan, Edelstein, Samuel, Liberman, Uri A
Published in The New England journal of medicine (15.01.1987)
Published in The New England journal of medicine (15.01.1987)
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Journal Article
Detection and incidence of anomalies associated with hypospadias
Friedman, Tal, Shalom, Avshalom, Hoshen, Guy, Brodovsky, Shlomo, Tieder, Martin, Westreich, Melvyn
Published in Pediatric nephrology (Berlin, West) (01.10.2008)
Published in Pediatric nephrology (Berlin, West) (01.10.2008)
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Journal Article
A Loss-of-Function Mutation in NaPi-IIa and Renal Fanconi's SyndromeBrief Report
Magen, Daniella, Berger, Liron, Coady, Michael J, Ilivitzki, Anat, Militianu, Daniela, Tieder, Martin, Selig, Sara, Lapointe, Jean Yves, Zelikovic, Israel, Skorecki, Karl
Published in The New England journal of medicine (25.03.2010)
Published in The New England journal of medicine (25.03.2010)
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Journal Article
SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaP^sub i^-IIc in Maintaining Phosphate Homeostasis
Bergwitz, Clemens, Roslin, Nicole M, Tieder, Martin, Loredo-Osti, J C
Published in American journal of human genetics (01.02.2006)
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Published in American journal of human genetics (01.02.2006)
Journal Article
Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene
JONES, Andrew O, TZENOVA, Jordana, RICE, Allan, ANDERSON, Donald, MORGAN, Kenneth, FUJIWARA, T. Mary, TENENHOUSE, Harriet S, FRAPPIER, Danielle, CRUMLEY, M. Joyce, ROSLIN, Nicole M, KOS, Claudine H, TIEDER, Martin, LANGMAN, Craig B, PROESMANS, Willem, CARPENTER, Thomas O
Published in Journal of the American Society of Nephrology (01.03.2001)
Published in Journal of the American Society of Nephrology (01.03.2001)
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Journal Article
Spondyloenchondrodysplasia: A rare cause of short-trunk syndrome
Robinson, Dror, Tieder, Martin, Copeliovitch, Leonel, Halperin, Nahum
Published in Acta orthopaedica (1991)
Published in Acta orthopaedica (1991)
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Journal Article
SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaP i-IIc in Maintaining Phosphate Homeostasis
Bergwitz, Clemens, Roslin, Nicole M., Tieder, Martin, Loredo-Osti, J.C., Bastepe, Murat, Abu-Zahra, Hilal, Frappier, Danielle, Burkett, Kelly, Carpenter, Thomas O., Anderson, Donald, Garabédian, Michèle, Sermet, Isabelle, Fujiwara, T. Mary, Morgan, Kenneth, Tenenhouse, Harriet S., Jüppner, Harald
Published in American journal of human genetics (2006)
Published in American journal of human genetics (2006)
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Journal Article
SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaOi-IIc in maintaining phosphate homeostasis
BERGWITZ, Clemens, ROSLIN, Nicole M, GARABEDIAN, Michèle, SERMET, Isabelle, FUJIWARA, T. Mary, MORGAN, Kenneth, TENENHOUSE, Harriet S, JUPPNER, Harald, TIEDER, Martin, LOREDO-OSTI, J. C, BASTEPE, Murat, ABU-ZAHRA, Hilal, FRAPPIER, Danielle, BURKETT, Kelly, CARPENTER, Thomas O, ANDERSON, Donald
Published in American journal of human genetics (2006)
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Published in American journal of human genetics (2006)
Journal Article
Hereditary Hypophosphatemic Rickets with Hypercalciuria: Report of a New Kindred
Sermet-Gaudelus, Isabelle, Garabédian, Michèle, Dechaux, Michèle, Lenoir, Gérard, Rey, Jean, Tieder, Martin
Published in Nephron (01.05.2001)
Published in Nephron (01.05.2001)
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Journal Article
Hereditary Hypophosphatemic Rickets with Hypercalciuria
Tieder, Martin, Modai, David, Samuel, Ruth, Arie, Raphael, Halabe, Aharon, Bab, Itai, Gabizon, Daniela, Liberman, Uri A
Published in The New England journal of medicine (07.03.1985)
Published in The New England journal of medicine (07.03.1985)
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Journal Article
Therapy-Resistant Seizures in Pseudohypoparathyroidism - A Case Report
Pollak, L., Klein, C., Tieder, M., Arlazoroff, A.
Published in Journal of Pediatric Endocrinology and Metabolism (01.07.1995)
Published in Journal of Pediatric Endocrinology and Metabolism (01.07.1995)
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