Mitchell-Riley syndrome: clinical analysis and investigation of molecular mechanisms

被引:0
|
作者
Duvillie, B. [1 ]
机构
[1] Inst Curie, CNRS, UMR 3347, Inserm,U1021, Orsay, France
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
下载
收藏
页码:121 / 121
页数:1
相关论文
共 50 条
  • [41] Molecular mechanisms of myelodysplastic syndrome
    Hirai, H
    JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2003, 33 (04) : 153 - 160
  • [42] Investigation into potential mechanisms of metabolic syndrome by integrative analysis of metabolomics and proteomics
    Chen, Meimei
    Yang, Zhaoyang
    Gan, Huijian
    Wang, Yang
    Li, Chandong
    Gao, Yuxing
    PLOS ONE, 2022, 17 (07):
  • [43] Natriuretic peptides and cardiovascular damage in the metabolic syndrome: molecular mechanisms and clinical implications
    Savoia, Carmine
    Volpe, Massimo
    Alonzo, Alessandro
    Rossi, Chiara
    Rubattu, Speranza
    CLINICAL SCIENCE, 2010, 118 (3-4) : 231 - 240
  • [44] Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome clinical features
    Pilarski, Robert
    Stephens, Julie A.
    Noss, Ryan
    Fisher, James L.
    Prior, Thomas W.
    JOURNAL OF MEDICAL GENETICS, 2011, 48 (08) : 505 - 512
  • [45] Clinical manifestations and molecular investigation of 50 patients with Williams syndrome in the Greek population
    Amenta, S
    Sofocleous, C
    Kolialexi, A
    Thomaidis, L
    Giouroukos, S
    Karavitakis, E
    Mavrou, A
    Kitsiou, S
    Kanavakis, E
    Fryssira, H
    PEDIATRIC RESEARCH, 2005, 57 (06) : 789 - 795
  • [46] Clinical Manifestations and Molecular Investigation of 50 Patients with Williams Syndrome in the Greek Population
    Stella Amenta
    Christalena Sofocleous
    Angeliki Kolialexi
    Loretta Thomaidis
    Sotiris Giouroukos
    Emmanuel Karavitakis
    Ariadni Mavrou
    Sophia Kitsiou
    Emmanuel Kanavakis
    Helen Fryssira
    Pediatric Research, 2005, 57 : 789 - 795
  • [47] The clinical, therapeutic and molecular genetic investigation of Birt-Hogg-Dube syndrome
    Lim, Derek
    Rehal, P. K.
    Kirby, G. A.
    MacDonald, F.
    Maher, E. R.
    JOURNAL OF MEDICAL GENETICS, 2009, 46 : S41 - S41
  • [48] INVESTIGATION OF LIQUEFACTION MECHANISMS WITH MOLECULAR PROBES
    BOCKRATH, BC
    SCHROEDER, KT
    SMITH, MR
    ENERGY & FUELS, 1989, 3 (02) : 268 - 272
  • [49] Clinical and molecular analysis of nine families with Adams–Oliver syndrome
    Pieter Verdyck
    Muriel Holder-Espinasse
    Wim Van Hul
    Wim Wuyts
    European Journal of Human Genetics, 2003, 11 : 457 - 463
  • [50] Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome
    Aslan, Pinar Gunay
    Caglayan, Ahmet Okay
    Bora, Elcin
    Koc, Altug
    Yucel, Hilal
    Ulgenalp, Ayfer
    Ozturk, Yesim
    Seker, Gul
    Akarsu, Mesut
    TURKISH JOURNAL OF GASTROENTEROLOGY, 2024, 35 (05): : 374 - 384