Literature DB >> 34731311

Amenorrhea in a pediatric kidney transplant recipient: Answers.

Benjamin Steinman1, Stella Kilduff1, Marcela Del Rio1, Nicole Hayde2.   

Abstract

Entities:  

Keywords:  Amenorrhea; Focal segmental glomerulosclerosis; Frasier syndrome; Kidney transplantation; Puberty

Year:  2021        PMID： 34731311     DOI： 10.1007/s00467-021-05320-4

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


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  12 in total

1.  GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS.

Authors:  S D FRASIER; R A BASHORE; H D MOSIER
Journal:  J Pediatr       Date:  1964-05       Impact factor: 4.406

2.  Secondary sexual characteristics and menses in young girls seen in office practice: a study from the Pediatric Research in Office Settings network.

Authors:  M E Herman-Giddens; E J Slora; R C Wasserman; C J Bourdony; M V Bhapkar; G G Koch; C M Hasemeier
Journal:  Pediatrics       Date:  1997-04       Impact factor: 7.124

Review 3.  Steroidogenic organ development and homeostasis: A WT1-centric view.

Authors:  Roberto Bandiera; Sonia Sacco; Valerie P I Vidal; Marie-Christine Chaboissier; Andreas Schedl
Journal:  Mol Cell Endocrinol       Date:  2015-01-14       Impact factor: 4.102

4.  Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy.

Authors:  Yo Han Ahn; Eu Jin Park; Hee Gyung Kang; Seong Heon Kim; Hee Yeon Cho; Jae Il Shin; Joo Hoon Lee; Young Seo Park; Kyo Sun Kim; Il-Soo Ha; Hae Il Cheong
Journal:  Pediatr Nephrol       Date:  2016-06-14       Impact factor: 3.714

5.  Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

Authors:  B Klamt; A Koziell; F Poulat; P Wieacker; P Scambler; P Berta; M Gessler
Journal:  Hum Mol Genet       Date:  1998-04       Impact factor: 6.150

Review 6.  WT1 and glomerular diseases.

Authors:  Patrick Niaudet; Marie-Claire Gubler
Journal:  Pediatr Nephrol       Date:  2006-08-23       Impact factor: 3.714

7.  Analysis of the Wilms' tumor suppressor gene (WT1) in patients 46,XY disorders of sex development.

Authors:  B Köhler; H Biebermann; V Friedsam; J Gellermann; R F Maier; M Pohl; P Wieacker; O Hiort; A Grüters; H Krude
Journal:  J Clin Endocrinol Metab       Date:  2011-04-20       Impact factor: 5.958

8.  Donor splice-site mutations in WT1 are responsible for Frasier syndrome.

Authors:  S Barbaux; P Niaudet; M C Gubler; J P Grünfeld; F Jaubert; F Kuttenn; C N Fékété; N Souleyreau-Therville; E Thibaud; M Fellous; K McElreavey
Journal:  Nat Genet       Date:  1997-12       Impact factor: 38.330

9.  Gonadoblastoma and dysgerminoma associated with XY gonadal dysgenesis in an adolescent with chronic renal failure: a case of Frasier syndrome.

Authors:  Minna M Joki-Erkkilä; Riitta Karikoski; Immo Rantala; Hanna-Liisa Lenko; Tapio Visakorpi; Pentti K Heinonen
Journal:  J Pediatr Adolesc Gynecol       Date:  2002-06       Impact factor: 1.814

10.  A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.

Authors:  Carolin E Sadowski; Svjetlana Lovric; Shazia Ashraf; Werner L Pabst; Heon Yung Gee; Stefan Kohl; Susanne Engelmann; Virginia Vega-Warner; Humphrey Fang; Jan Halbritter; Michael J Somers; Weizhen Tan; Shirlee Shril; Inès Fessi; Richard P Lifton; Detlef Bockenhauer; Sherif El-Desoky; Jameela A Kari; Martin Zenker; Markus J Kemper; Dominik Mueller; Hanan M Fathy; Neveen A Soliman; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2014-10-27       Impact factor: 10.121
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