检索结果 - Rajesh V. Thakker

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  1. 1
    Multiple Endocrine Neoplasia—Syndromes of the Twentieth Century

    Multiple Endocrine Neoplasia—Syndromes of the Twentieth Century 由 Rajesh V. Thakker

    出版 1998
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  2. 2
    Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4)

    Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4) 由 Rajesh V. Thakker

    出版 2013
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  3. 3
    Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis

    Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis 由 Rajesh V. Thakker

    出版 2000
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  4. 4
    Genetics of parathyroid tumours

    Genetics of parathyroid tumours 由 Rajesh V. Thakker

    出版 2016
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  5. 5
    Dent's disease

    Dent's disease 由 Olivier Devuyst, Rajesh V. Thakker

    出版 2010
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  6. 6
    <i>GNAS</i> Mutations in Pseudohypoparathyroidism Type 1a and Related Disorders

    <i>GNAS</i> Mutations in Pseudohypoparathyroidism Type 1a and Related Disorders 由 Manuel C. Lemos, Rajesh V. Thakker

    出版 2014
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  7. 7
    Somatic Mutations in MEN Type 1 Tumors, Consistent with the Knudson “Two-Hit” Hypothesis

    Somatic Mutations in MEN Type 1 Tumors, Consistent with the Knudson “Two-Hit” Hypothesis 由 A. A. J. Pannett, Rajesh V. Thakker

    出版 2001
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  8. 8
    Multiple endocrine neoplasia type 1.

    Multiple endocrine neoplasia type 1. 由 A. A. J. Pannett, Rajesh V. Thakker

    出版 1999
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  9. 9
    Disorders of the calcium-sensing receptor and partner proteins: insights into the molecular basis of calcium homeostasis

    Disorders of the calcium-sensing receptor and partner proteins: insights into the molecular basis of calcium homeostasis 由 Fadil Hannan, Valerie Babinsky, Rajesh V. Thakker

    出版 2016
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  10. 10
    Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma

    Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma 由 Luís Cardoso, Mark Stevenson, Rajesh V. Thakker

    出版 2017
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  11. 11
    Parafibromin – functional insights

    Parafibromin – functional insights 由 Paul Newey, Michael R. Bowl, Rajesh V. Thakker

    出版 2009
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  12. 12
    Genetic causes of hypercalciuric nephrolithiasis

    Genetic causes of hypercalciuric nephrolithiasis 由 Michael Stechman, Nellie Y. Loh, Rajesh V. Thakker

    出版 2008
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  13. 13
    Current and emerging therapies for PNETs in patients with or without MEN1

    Current and emerging therapies for PNETs in patients with or without MEN1 由 Morten Frost, Kate E Lines, Rajesh V. Thakker

    出版 2018
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  14. 14
    Genetics of hereditary forms of primary hyperparathyroidism

    Genetics of hereditary forms of primary hyperparathyroidism 由 Katherine English, Kate E Lines, Rajesh V. Thakker

    出版 2023
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  15. 15
    Cell division cycle protein 73 homolog (<i>CDC73</i>) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors

    Cell division cycle protein 73 homolog (<i>CDC73</i>) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors 由 Paul Newey, Michael R. Bowl, Treena Cranston, Rajesh V. Thakker

    出版 2010
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  16. 16
    Hypercalcemic Disorders in Children

    Hypercalcemic Disorders in Children 由 Victoria Stokes, Morten Frost Nielsen, Fadil Hannan, Rajesh V. Thakker

    出版 2017
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  17. 17
    Genetics of neuroendocrine and carcinoid tumours.

    Genetics of neuroendocrine and carcinoid tumours. 由 Poloko D. Leotlela, A. Jauch, H Holtgreve-Grez, Rajesh V. Thakker

    出版 2003
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  18. 18
    Structure and methylation of the human calcitonin/α-CGRP gene

    Structure and methylation of the human calcitonin/α-CGRP gene 由 P.M. Broad, Aviva J. Symes, Rajesh V. Thakker, R K Craig

    出版 1989
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  19. 19
    The calcium-sensing receptor in physiology and in calcitropic and noncalcitropic diseases

    The calcium-sensing receptor in physiology and in calcitropic and noncalcitropic diseases 由 Fadil Hannan, Enikö Kállay, Wenhan Chang, Maria Luisa Brandi, Rajesh V. Thakker

    出版 2018
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  20. 20
    Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families.

    Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families. 由 Philip L. Beales, Alison Warner, G. A. Hitman, Rajesh V. Thakker, Frances Flinter

    出版 1997
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