Literature DB >> 14112243

HYPOGONADOTROPHIC HYPOGONADISM IN THE LAURENCE-MOON SYNDROME.

R F REINFRANK, F L NICHOLS.   

Abstract

Keywords:  GENETICS, HUMAN; GONADOTROPINS; HYPOGONADISM; LAURENCE-MOON-BIEDL SYNDROME; PATHOLOGY; TESTIS; URINE

Mesh：

Substances：

Year:  1964        PMID： 14112243     DOI： 10.1210/jcem-24-1-48

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN： 0021-972X            Impact factor:   5.958


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  5 in total

1.  [Defects and excess in Laurence-Moon-Bardet-Biedl syndrome].

Authors:  G Jacobi
Journal:  Z Kinderheilkd       Date:  1965-10-11

2.  Familial hypothalamic hypogonadotropic hypogonadism.

Authors:  R Matte; P D'Amour; C Faiman; J S Winter
Journal:  Can Med Assoc J       Date:  1974-03-02       Impact factor: 8.262

3.  Familial hypogonadotropic hypogonadism with alopecia.

Authors:  I S Slti; Z Salem
Journal:  Can Med Assoc J       Date:  1979-08-18       Impact factor: 8.262

4.  BBS4 protein has basal body/ciliary localization in sensory organs but extra-ciliary localization in oligodendrocytes during human development.

Authors:  K Bénardais; G Delfino; B Samama; D Devys; M C Antal; M S Ghandour; N Boehm
Journal:  Cell Tissue Res       Date:  2021-04-16       Impact factor: 5.249

5.  Reproduction Function in Male Patients With Bardet Biedl Syndrome.

Authors:  Isabelle Koscinski; Manuel Mark; Nadia Messaddeq; Jean-Jacques Braun; Catherine Celebi; Jean Muller; Anna Zinetti-Bertschy; Nathalie Goetz; Hélène Dollfus; Sylvie Rossignol
Journal:  J Clin Endocrinol Metab       Date:  2020-12-01       Impact factor: 5.958
  5 in total

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