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Literature DB >> 11686549

Pseudohypoparathyroidism with normocalcemia.

N Ozbey.

Abstract

Entities: Disease

Mesh：

Substances：
Calcium

Year: 2001 PMID： 11686549 DOI： 10.1007/BF03343907

Source DB: PubMed Journal: J Endocrinol Invest ISSN： 0391-4097 Impact factor: 4.256

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12 in total

Review 1. Clinical implications of genetic defects in G proteins. The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy.

Authors: M D Ringel; W F Schwindinger; M A Levine
Journal: Medicine (Baltimore) Date: 1996-07 Impact factor: 1.889

2. Normal parathyroid hormone responsiveness of bone-derived cells from a patient with pseudohypoparathyroidism.

Authors: S Ish-Shalom; L G Rao; M A Levine; D Fraser; S W Kooh; R G Josse; R McBroom; M M Wong; T M Murray
Journal: J Bone Miner Res Date: 1996-01 Impact factor: 6.741

3. Heterogeneous mutations in the gene encoding the alpha-subunit of the stimulatory G protein of adenylyl cyclase in Albright hereditary osteodystrophy.

Authors: A Miric; J D Vechio; M A Levine
Journal: J Clin Endocrinol Metab Date: 1993-06 Impact factor: 5.958

Review 4. Albright's hereditary osteodystrophy: a review.

Authors: N Fitch
Journal: Am J Med Genet Date: 1982-01

5. The development of pseudohypoparathyroidism. Involvement of progressively increasing serum parathyroid hormone concentrations, increased 1,25-dihydroxyvitamin D concentrations, and 'migratory' subcutaneous calcifications.

Authors: R C Tsang; P Venkataraman; M Ho; J J Steichen; J Whitsett; F Greer
Journal: Am J Dis Child Date: 1984-07

2. Pseudohypoparathyroidism Type 1A with Normocalcaemia, due to the Novel C.389A>G Variant of Exon 5 of the Guanine Nucleotide-Binding Protein, α-Stimulating Gene.

Authors: Eleni P Kotanidou; Vasiliki-Rengina Tsinopoulou; Anastasios Serbis; Eleni Litou; Assimina Galli-Tsinopoulou
Journal: J Bone Metab Date: 2021-02-28

2 in total

Pseudohypoparathyroidism with normocalcemia.

Review 1. Clinical implications of genetic defects in G proteins. The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy.

2. Normal parathyroid hormone responsiveness of bone-derived cells from a patient with pseudohypoparathyroidism.

3. Heterogeneous mutations in the gene encoding the alpha-subunit of the stimulatory G protein of adenylyl cyclase in Albright hereditary osteodystrophy.

Review 4. Albright's hereditary osteodystrophy: a review.

5. The development of pseudohypoparathyroidism. Involvement of progressively increasing serum parathyroid hormone concentrations, increased 1,25-dihydroxyvitamin D concentrations, and 'migratory' subcutaneous calcifications.

6. Studies on the attainment of normocalcemia in patients with pseudohypoparathyroidism.

7. Pseudohypoparathyroidism--another monogenic obesity syndrome.

8. A 4-base pair deletion mutation of Gs alpha gene in a Japanese patient with pseudohypoparathyroidism.

Review 9. Pseudohypoparathyroidism. New insights into an old disease.

10. Relationship of estrogen and pregnancy to calcium homeostasis in pseudohypoparathyroidism.

1. Identification of a novel GNAS mutation in a case of pseudohypoparathyroidism type 1A with normocalcemia.

2. Pseudohypoparathyroidism Type 1A with Normocalcaemia, due to the Novel C.389A>G Variant of Exon 5 of the Guanine Nucleotide-Binding Protein, α-Stimulating Gene.