RJ Ferland, JN Gaitanis, K Apse, U … - American journal of medical genetics. Part A, 2006 - walshlab.org Russell J. Ferland,1 John N. Gaitanis,2 Kira Apse,3 Umadevi Tantravahi,4
Christopher A. Walsh,3,5 and Volney L. Sheen3* 1Department of Biology,
Rensselaer Polytechnic Institute, Center for Biotechnology and ... Cited by 16 - Related articles - View as HTML - BL Direct - All 5 versions
- ►walshlab.org [PDF] RJ Ferland, LF Batiz, J Neal, G Lian, E … - Human Molecular Genetics, 2009 - Oxford Univ Press Impairments in neuronal migration, particularly in cell motility, are thought to
give rise to several genetic malformations of the developing cortex:
lissencephaly (smooth brain), subcortical band heterotopia (heterotopic ... Cited by 7 - Related articles - All 5 versions
- ►univ-mrs.fr [PDF] C Cardoso, A Boys, E Parrini, C Mignon-Ravix, … - Neurology, 2009 - AAN Enterprises From INSERM U901 (CC, SK), INMED, University de la Méditerranee, Campus de
Luminy, Marseille, France; INSERM U491 (CC, CM-R., EP, LV), University de la
Méditerranee, Faculte de Medecine La Timone, Marseille; Victorian Clinical ... Cited by 7 - Related articles - All 4 versions
E Bodó, A Kromminga, T Bíró, I Borbíró, E … - Journal of Investigative Dermatology, 2008 - nature.com Pituitary thyroid-stimulating hormone (TSH) regulates thyroid hormone synthesis
via receptors (TSH-R) expressed on thyroid epithelial cells. As the hair
follicle (HF) is uniquely hormone-sensitive and, hypothyroidism with its ... Cited by 4 - Related articles - All 4 versions
MCY de Wit, JM Kros, DJJ Halley, IFM de Coo … - British Medical Journal, 2009 - jnnp.bmj.com Filamin A is an important gene involved in the development of the brain, heart,
connective tissue and blood vessels. A case is presented illustrating the
challenge in recognising patients with filamin A mutations. The patient, a ... Related articles - All 2 versions
G Sole, I Coupry, C Rooryck, E Guerineau, F … - Journal of Neurology, Neurosurgery & Psychiatry, 2009 - pt.wkhealth.com Bilateral periventricular nodular heterotopia (BPNH) is the most common form of
periventricular heterotopia. Mutations in FLNA, encoding filamin A, are
responsible for the X linked dominant form of BPNH (FLNA-BPNH). Recently, ...