Papers authored by Rajesh Thakker
Refreshing results…
2001
Aa A. J. Pannett,
L. Ruas,
Mm Ruas,
T. Krausz,
Santos,
Lg G. Sobrinho,
Leite,
Rv Thakker 
,
L. Barros,
M. Carvalheiro,
Bm M. Cavaco
,
L. Barros,
M. Carvalheiro,
Bm M. Cavaco
The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred.
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D. Hunter,
M. De Lange,
H. Snieder,
Aj J. MacGregor,
R. Swaminathan,
Rv V. Thakker ,
Td D. Spector
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,
Td D. Spector
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K. Trautmann,
R. V. Thakker ,
D. W. Ellison,
A. Ibrahim,
P. D. Lees,
B. Harding,
C. Fischer,
S. Popp,
C. R. Bartram,
A. Jauch
,
D. W. Ellison,
A. Ibrahim,
P. D. Lees,
B. Harding,
C. Fischer,
S. Popp,
C. R. Bartram,
A. Jauch
Chromosomal aberrations in sporadic pituitary tumors
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Maria Luisa Brandi,
Samuel A. Wells,
Robert F. Gagel,
Alberto Angeli,
John P. Bilezikian,
Paolo Beck-Peccoz,
Cesare Bordi,
Bernard Conte-Devolx,
Alberto Falchetti,
Riccardo Gionata Gheri,
Alfonso Libroia,
Cornelius J. M. Lips,
Gaetano Lombardi,
Massimo Mannelli,
Furio Pacini
and 10 other authors
Consensus: Guidelines for diagnosis and therapy of MEN type 1 and type 2
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2000
Ss Wang,
Ys Wang,
Xt Wang,
S. S. Wang,
X.-T. Wang,
Y. Wang,
Olivier Devuyst,
Pj J. Courtoy,
H. Wang,
Rv Thakker ,
S. Guggino,
Wb B. Guggino
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,
S. Guggino,
Wb B. Guggino
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Te E. Willnow,
Rv V. Thakker ,
Pj J. Verroust,
Christian Jacobsen,
Ag G. W. Norden,
Ei I. Christensen,
Sk K. Moestrup,
Mm M. Sousa,
Mj J. Saraiva
,
Pj J. Verroust,
Christian Jacobsen,
Ag G. W. Norden,
Ei I. Christensen,
Sk K. Moestrup,
Mm M. Sousa,
Mj J. Saraiva
Evidence for the role of megalin in renal uptake of transthyretin.
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Katsusuke Yamamoto,
Jeremy P. D. T. Cox,
Thomas Friedrich,
Paul T. Christie,
Martin Bald,
Peter N. Houtman,
Marta J. Lapsley,
Ludwig Patzer,
Michel Tsimaratos,
William G. Van'T Hoff,
Kanji Yamaoka,
Thomas J. Jentsch,
Rajesh V. Thakker
Characterization of renal chloride channel (CLCN5) mutations in Dent's disease
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Pt T. Christie,
Aa A. J. Pannett,
Rv Thakker ,
Michael P. Whyte,
Patrick Finnegan,
Jonathan Jones,
Ph H. Dixon,
Brian Harding,
Steven Mumm,
Gs S. Gottesman
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,
Michael P. Whyte,
Patrick Finnegan,
Jonathan Jones,
Ph H. Dixon,
Brian Harding,
Steven Mumm,
Gs S. Gottesman
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Hilde Van Esch ,
H. van Esch,
W. van de Ven,
Peter Groenen,
M. Andrew Nesbit,
Simone Schuffenhauer,
Peter Lichtner,
M. Andrew Nesbit,
Gert Vanderlinden,
Brian Harding,
Rolf Beetz,
Rudolf W. Bilous,
Ian Holdaway,
Nicholas J. Shaw,
Jean-Pierre Fryns
and 3 other authors
,
H. van Esch,
W. van de Ven,
Peter Groenen,
M. Andrew Nesbit,
Simone Schuffenhauer,
Peter Lichtner,
M. Andrew Nesbit,
Gert Vanderlinden,
Brian Harding,
Rolf Beetz,
Rudolf W. Bilous,
Ian Holdaway,
Nicholas J. Shaw,
Jean-Pierre Fryns
and 3 other authors
GATA3 haplo-insufficiency causes human HDR syndrome.
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Jp Cox,
Katsusuke Yamamoto,
Pt Christie,
Carol Wooding,
Terry Feest,
Fa Flinter,
Pr Goodyer,
Ernst Leumann,
Thomas Neuhaus,
Christopher Reid,
Pf Williams,
Oliver Wrong,
Rv Thakker
Renal chloride channel, CLCN5, mutations in Dent's disease.
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