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Literature DB >> 14431322

True idiopathic hypoparathyroidism as a sexlinked recessive trait.

V H PEDEN.

Abstract

Entities: Disease

Keywords: PARATHYROID GLANDS/diseases

Mesh：

Year: 1960 PMID： 14431322 PMCID： PMC1932250

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

× No keyword cloud information.

21 in total

1. Sporadic or non-endemic familial cretinism with goiter.

Authors: J B STANBURY; E M MCGIRR
Journal: Am J Med Date: 1957-05 Impact factor: 4.965

2. [Not Available].

Authors: S BUCHS
Journal: Ann Paediatr Date: 1957-02

3. The syndrome of familial juvenile hypoadrenocorticism, hypoparathyroidism and superficial moniliasis.

Authors: V M ESSELBORN; B H LANDING; J WHITAKER; R R WILLIAMS
Journal: J Clin Endocrinol Metab Date: 1956-10 Impact factor: 5.958

4. Idiopathic hypoparathyroidism and Addison's disease.

Authors: R R ELLISON; A R KANTROWITZ; L NORSA; M PERLMUTTER
Journal: Am J Med Date: 1956-10 Impact factor: 4.965

5. [Not Available].

Authors: S BUCHS
Journal: Ann Paediatr Date: 1955-06

6. Pseudo-hypoparathyroidism; a description of three cases and a critical appraisal of earlier accounts of the disease.

Authors: M E MACGREGOR; T P WHITEHEAD
Journal: Arch Dis Child Date: 1954-10 Impact factor: 3.791

7. [Tetany syndrome and general underdevelopment in an infant with congenital absence of the parathyroid].

Authors: A BLAIM; Z LEWICKI
Journal: Pediatr Pol Date: 1955-09

8. Addison's disease in a boy with hypoparathyroidism.

Authors: C PAPADATOS; R KLEIN
Journal: J Clin Endocrinol Metab Date: 1954-06 Impact factor: 5.958

9. Idiopathic hypoparathyroidism and chronic adrenal insufficiency: a case report.

Authors: E LEIFER; W HOLLANDER
Journal: J Clin Endocrinol Metab Date: 1953-10 Impact factor: 5.958

10. Familial hypoparathyroidism; report of a case.

Authors: R GOLDMAN; J L REYNOLDS; H R CUMMINGS; S H BASSETT
Journal: J Am Med Assoc Date: 1952-11-15

14 in total

1. Long-standing latent idiopathic hypoparathyroidism discovered during concurrent central nervous system disease.

Authors: B E Wilson; S Tawney
Journal: West J Med Date: 1992-08

Review 2. Molecular genetics of mineral metabolic disorders.

Authors: R V Thakker
Journal: J Inherit Metab Dis Date: 1992 Impact factor: 4.982

Review 3. Gene mapping of mineral metabolic disorders.

Authors: R V Thakker; K E Davies; J L O'Riordan
Journal: J Inherit Metab Dis Date: 1989 Impact factor: 4.982

4. Primary familial hypoparathyroidism with an autosomal dominant mode of inheritance.

Authors: C De Campo; L Piscopello; C Noacco; P Da Col; G C Englaro; A Benedetti
Journal: J Endocrinol Invest Date: 1988-02 Impact factor: 4.256

5. Male triplets concordant for X-linked recessive nonsyndromic hypoparathyroidism.

Authors: A S Teebi; A R Kishawi; A H Malek
Journal: Eur J Pediatr Date: 1992-06 Impact factor: 3.183

6. Craniofacioskeletal syndrome: an X-linked dominant disorder with early lethality in males.

Authors: Roger E Stevenson; Cam K Brasington; Cindy Skinner; Richard J Simensen; J Edward Spence; Shelli Kesler; Allan L Reiss; Charles E Schwartz
Journal: Am J Med Genet A Date: 2007-10-01 Impact factor: 2.802

7. mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation.

Authors: S Mumm; M P Whyte; R V Thakker; K H Buetow; D Schlessinger
Journal: Am J Hum Genet Date: 1997-01 Impact factor: 11.025