Literature DB >> 7939840

Case report 848. Kallman's syndrome: hypogonadotropic hypogonadism with delayed closure of epiphyseal growth zones, resulting in epiphysiolysis of the left proximal femoral epiphysis after trauma.

H A Vallier1, A G Bergman, S A Kargas.   

Abstract

Entities:  

Mesh：

Year:  1994        PMID： 7939840     DOI： 10.1007/bf02416999

Source DB:  PubMed          Journal:  Skeletal Radiol        ISSN： 0364-2348            Impact factor:   2.199


× No keyword cloud information.
  13 in total

Review 1.  Pituitary gigantism.

Authors:  W H Daughaday
Journal:  Endocrinol Metab Clin North Am       Date:  1992-09       Impact factor: 4.741

2.  A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.

Authors:  B Franco; S Guioli; A Pragliola; B Incerti; B Bardoni; R Tonlorenzi; R Carrozzo; E Maestrini; M Pieretti; P Taillon-Miller; C J Brown; H F Willard; C Lawrence; M Graziella Persico; G Camerino; A Ballabio
Journal:  Nature       Date:  1991-10-10       Impact factor: 49.962

Review 3.  Syndrome of anosmia with hypogonadotropic hypogonadism (Kallmann syndrome): clinical and laboratory studies in 23 cases.

Authors:  J M Lieblich; A D Rogol; B J White; S W Rosen
Journal:  Am J Med       Date:  1982-10       Impact factor: 4.965

4.  The ultrastructure of the growth plate in slipped capital femoral epiphysis.

Authors:  M R Mickelson; I V Ponseti; R R Cooper; J A Maynard
Journal:  J Bone Joint Surg Am       Date:  1977-12       Impact factor: 5.284

Review 5.  Puberty and its disorders in boys.

Authors:  D M Styne
Journal:  Endocrinol Metab Clin North Am       Date:  1991-03       Impact factor: 4.741

6.  Growth pattern of boys with isolated gonadotropin deficiency.

Authors:  A Kaushanski; Z Laron
Journal:  Isr J Med Sci       Date:  1979-06

Review 7.  Radiologic manifestations in the musculoskeletal system of miscellaneous endocrine disorders.

Authors:  F S Chew
Journal:  Radiol Clin North Am       Date:  1991-01       Impact factor: 2.303

8.  The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.

Authors:  R Legouis; J P Hardelin; J Levilliers; J M Claverie; S Compain; V Wunderle; P Millasseau; D Le Paslier; D Cohen; D Caterina
Journal:  Cell       Date:  1991-10-18       Impact factor: 41.582

9.  Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.

Authors:  T Meitinger; B Heye; C Petit; J Levilliers; A Golla; C Moraine; B Dalla Piccola; W G Sippell; J Murken; A Ballabio
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025

10.  The effect of pubertal delay on adult height in men with isolated hypogonadotropic hypogonadism.

Authors:  M M Uriarte; J Baron; H B Garcia; K M Barnes; D L Loriaux; G B Cutler
Journal:  J Clin Endocrinol Metab       Date:  1992-02       Impact factor: 5.958
View more
  1 in total

1.  Incidentally Detected Juvenile-Pattern Bone Scintigraphy in a Young Man with Kallmann's Syndrome.

Authors:  Soo Hyun Kwon; Yoon-Sok Chung; Dong Hyun Lee; Kyung-Sook Jo; Young-Sil An; Joon-Kee Yoon; Su Jin Lee
Journal:  Nucl Med Mol Imaging       Date:  2014-02-15
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.