Suchergebnisse - "Simonds, W F"

PubPharm (74)

1

Denosumab-Induced Prolonged Hypocalcemia and Hypophosphatemia in Three Patients With Severe Primary Hyperparathyroidism and Renal Insufficiency

enthalten in: Journal of clinical densitometry | 2014

von Yavuz, S. | Diker-Cohen, T. | Marx, S. | +3

2

The EIF4EBP3 translational repressor is a marker of CDC73 tumor suppressor haploinsufficiency in a parathyroid cancer syndrome

enthalten in: Cell death & disease | 2012

von Zhang, J. | Seigneur, E. | Pandey, M. | +6

3

Cytoplasmic polyadenylation element binding protein is a conserved target of tumor suppressor HRPT2/CDC73

enthalten in: Cell death and differentiation | 2010

von Zhang, J. | Panicker, L. | Seigneur, E. | +8

4

Cytoplasmic polyadenylation element binding protein is a conserved target of tumor suppressor HRPT2/CDC73

enthalten in: Cell death & differentiation | 2010

von Zhang, J. | Panicker, L. | Seigneur, E. | +8

5

CLINICAL VIGNETTE - Surveillance for Early Detection of Aggressive Parathyroid Disease: Carcinoma and Atypical Adenoma in Familial Isolated Hyperparathyroidism Associated With a Germline HRPT2 Mutation - Familial hyperparathyroid syndromes involving mutations of HRPT2 (also CDC73), a tumor suppressor, are important to identify because the relatively high incidence of parathyroid malignancy associated with such mutations warrants a specific surveillance strategy. However, there is a dearth of reports describing experience with surveillance and early detection informed by genetic insight into this disorder.

enthalten in: Journal of bone and mineral research | 2006

von Kelly, T. | Shattuck, T. | Reyes-Mugica, M. | +5

6

Endocrine Care - Of Special Interest to the Practice of Endocrinology - Familial Isolated Hyperparathyroidism Is Rarely Caused by Germline Mutation in HRPT2, the Gene for the Hyperparathyroidism-Jaw Tumor Syndrome

enthalten in: The journal of clinical endocrinology & metabolism | 2004

von Simonds, W. | Robbins, C. | Agarwal, S. | +3

7

Endocrine Care Of Special Interest to the Practice of Endocrinology - Multiple Endocrine Neoplasia Type 1 Variant with Frequent Prolactinoma and Rare Gastrinoma

enthalten in: The journal of clinical endocrinology & metabolism | 2004

von Hao, W. | Skarulis, M. | Simonds, W. | +6

8

PERSPECTIVE - HRPT2, a Marker of Parathyroid Cancer

enthalten in: The New England journal of medicine | 2003

von Weinstein, L. | Simonds, W.

9

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome

enthalten in: Nature genetics | 2002

von Carpten, J. | Robbins, C. | Villablanca, A. | +38

10

Hyperparathyroidism in Hereditary Syndromes: Special Expressions and Special Managements

enthalten in: Journal of bone and mineral research | 2002

von Marx, S. | Simonds, W. | Agarwal, S. | +11

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