scholarly journals EP08.07: Measurement of Sylvian fissure angles at 18-30 weeks' gestation in cases with neuronal migration disorder

2018 ◽  
Vol 52 ◽  
pp. 223-223
Author(s):  
R.K. Pooh ◽  
T. Nakamura ◽  
M. Machida ◽  
K. Uenishi ◽  
K. Kusunoki ◽  
...  
Keyword(s):  
Neuronal Migration ◽  
Sylvian Fissure ◽  
Neuronal Migration Disorder ◽  
Migration Disorder

Bilateral central macrogyria: Epilepsy, pseudobulbar palsy, and mental retardation?a recognizable neuronal migration disorder

1989 ◽  
Vol 25 (6) ◽  
pp. 547-554 ◽  
Author(s):  
Ruben Kuzniecky ◽  
Frederick Andermann ◽  
Donatella Tampieri ◽  
Denis Melanson ◽  
Andre Olivier ◽  
...  
Keyword(s):  
Mental Retardation ◽  
Neuronal Migration ◽  
Pseudobulbar Palsy ◽  
Neuronal Migration Disorder ◽  
Migration Disorder

Sudden death in a patient with mosaic ring X Turner syndrome and a neuronal migration disorder

2008 ◽  
Vol 17 (1) ◽  
pp. 69-71
Author(s):  
Cheryl Longman ◽  
James MacKenzie ◽  
Rosslyn Rankin ◽  
Meriel McEntagart ◽  
Richard Johnson ◽  
...  
Keyword(s):  
Sudden Death ◽  
Turner Syndrome ◽  
Neuronal Migration ◽  
Neuronal Migration Disorder ◽  
Migration Disorder

Olfactory bulb dysplasia: A novel subtype of neuronal migration disorder

1999 ◽  
Vol 46 (5) ◽  
pp. 783-786 ◽  
Author(s):  
Hideo Yamanouchi ◽  
Junko Hirato ◽  
Hideaki Yokoo ◽  
Yasushi Nako ◽  
Akihiro Morikawa ◽  
...  
Keyword(s):  
Olfactory Bulb ◽  
Neuronal Migration ◽  
Neuronal Migration Disorder ◽  
Migration Disorder

scholarly journals CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration

Endocrinology ◽  
2016 ◽  
Vol 157 (5) ◽  
pp. 1956-1966 ◽  
Author(s):  
B. Ian Hutchins ◽  
L. Damla Kotan ◽  
Carol Taylor-Burds ◽  
Yusuf Ozkan ◽  
Paul J. Cheng ◽  
...  
Keyword(s):  
Neuronal Migration ◽  
Novel Mutation ◽  
Hypogonadotropic Hypogonadism ◽  
Coiled Coil ◽  
Reproductive Function ◽  
Kallmann Syndrome ◽  
System A ◽  
Neuronal Migration Disorder ◽  
Gnrh Neurons ◽  
Migration Disorder

Abstract The first mutation in a gene associated with a neuronal migration disorder was identified in patients with Kallmann Syndrome, characterized by hypogonadotropic hypogonadism and anosmia. This pathophysiological association results from a defect in the development of the GnRH and the olfactory system. A recent genetic screening of Kallmann Syndrome patients revealed a novel mutation in CCDC141. Little is known about CCDC141, which encodes a coiled-coil domain containing protein. Here, we show that Ccdc141 is expressed in GnRH neurons and olfactory fibers and that knockdown of Ccdc141 reduces GnRH neuronal migration. Our findings in human patients and mouse models predict that CCDC141 takes part in embryonic migration of GnRH neurons enabling them to form a hypothalamic neuronal network to initiate pulsatile GnRH secretion and reproductive function.

scholarly journals A Behavioral Evaluation of Sex Differences in a Mouse Model of Severe Neuronal Migration Disorder

PLoS ONE ◽  
2013 ◽  
Vol 8 (9) ◽  
pp. e73144 ◽  
Author(s):  
Dongnhu T. Truong ◽  
Ashley Bonet ◽  
Amanda R. Rendall ◽  
Glenn D. Rosen ◽  
Roslyn H. Fitch
Keyword(s):  
Sex Differences ◽  
Mouse Model ◽  
Neuronal Migration ◽  
Neuronal Migration Disorder ◽  
Migration Disorder

scholarly journals NEURONAL MIGRATION DISORDER – A CLINICAL CASE

2015 ◽  
Vol 64 (3) ◽  
pp. 297-299
Author(s):  
Carmen Voicila ◽  
◽  
Anca Cabat ◽  
Raluca Gabriela Ioan ◽  
◽  
...  
Keyword(s):  
Respiratory Distress ◽  
Neuronal Migration ◽  
Clinical Case ◽  
Muscle Tone ◽  
Porencephalic Cyst ◽  
Fetal Infection ◽  
Neonatal Respiratory Distress ◽  
Neuronal Migration Disorder ◽  
Periventricular Heterotopia ◽  
Migration Disorder

The authors present the case of a newborn transferred to the Neonatology Section of IOMC Polizu, 43 hours after birth suffering from syndrome of neonatal respiratory distress and suspicion of maternal – fetal infection, extensively investigated during hospitalization for persistency of muscle tone disorder which could not be explained by asphyxia at birth, diagnosed after MRI with right periventricular heterotopia associated with left temporal porencephalic cyst and schizencephaly on the same side.

scholarly journals Localised neuronal migration disorder and intractable epilepsy: a prenatal vascular aetiology.

1993 ◽  
Vol 56 (3) ◽  
pp. 314-316 ◽  
Author(s):  
D C Reutens ◽  
S F Berkovic ◽  
R M Kalnins ◽  
P McKelvie ◽  
M M Saling ◽  
...  
Keyword(s):  
Neuronal Migration ◽  
Intractable Epilepsy ◽  
Neuronal Migration Disorder ◽  
Migration Disorder
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