Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency
In this case report we assess the occurrence of cortical malformations in children with early infant...
ObjectiveTwo unrelated families were ascertained in which sisters had infantile onset of epilepsy an...
AbstractPurposeMutations in PCDH19, encoding protocadherin 19 on chromosome X, cause familial epilep...
Protocadherin 19 (PCDH19) female limited epilepsy (PCDH19-FE; also known as epilepsy and mental reta...
To explore the causative role of PCDH19 gene (Xq22) in female patients with epilepsy
Epilepsy and mental retardation limited to females (EFMR) is a disorder with an X-linked mode of inh...
Mutations in PCDH19, which encodes protocadherin 19, have been identified in epilepsy, mainly in aff...
Aim: The inherit base of PCDH19-related epilepsy suggests a hormonal involvement due to de-regulatio...
International audienceMutations in PCDH19, encoding protocadherin 19 on chromosome X, cause familial...
International audiencePCDH19 encodes protocadherin 19 on chromosome Xq22.3. This 1,148-amino-acid pr...
Patients affected by protocadherin 19 (PCDH19)\u2013female limited epilepsy (PCDH19- FE) present a r...
Background: Epilepsy and mental retardation limited to females (EFMR) is an intriguing X-linked diso...
Purpose: To describe clinical and neuropsychological features of six consecutive sporadic girls with...
Background and Aims:PCDH19 gene, which encodes protocadherin 19, is associated with epilepsy and int...
PCDH19-female epilepsy (PCDH19-FE) is a female-limited epilepsy characterised by a spectrum of neuro...
In this case report we assess the occurrence of cortical malformations in children with early infant...
ObjectiveTwo unrelated families were ascertained in which sisters had infantile onset of epilepsy an...
AbstractPurposeMutations in PCDH19, encoding protocadherin 19 on chromosome X, cause familial epilep...
Protocadherin 19 (PCDH19) female limited epilepsy (PCDH19-FE; also known as epilepsy and mental reta...
To explore the causative role of PCDH19 gene (Xq22) in female patients with epilepsy
Epilepsy and mental retardation limited to females (EFMR) is a disorder with an X-linked mode of inh...
Mutations in PCDH19, which encodes protocadherin 19, have been identified in epilepsy, mainly in aff...
Aim: The inherit base of PCDH19-related epilepsy suggests a hormonal involvement due to de-regulatio...
International audienceMutations in PCDH19, encoding protocadherin 19 on chromosome X, cause familial...
International audiencePCDH19 encodes protocadherin 19 on chromosome Xq22.3. This 1,148-amino-acid pr...
Patients affected by protocadherin 19 (PCDH19)\u2013female limited epilepsy (PCDH19- FE) present a r...
Background: Epilepsy and mental retardation limited to females (EFMR) is an intriguing X-linked diso...
Purpose: To describe clinical and neuropsychological features of six consecutive sporadic girls with...
Background and Aims:PCDH19 gene, which encodes protocadherin 19, is associated with epilepsy and int...
PCDH19-female epilepsy (PCDH19-FE) is a female-limited epilepsy characterised by a spectrum of neuro...
In this case report we assess the occurrence of cortical malformations in children with early infant...
ObjectiveTwo unrelated families were ascertained in which sisters had infantile onset of epilepsy an...
AbstractPurposeMutations in PCDH19, encoding protocadherin 19 on chromosome X, cause familial epilep...