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De novo mutations of voltage-gated sodium channel α II gene SCN2A in intractable epilepsies

Neurology, 2009-09, Vol.73 (13), p.1046-1053

2009

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Intraoperative sonographic detection of ureteral jet during uncomplicated Cesarean delivery is feasible and safe

Ultrasound in obstetrics & gynecology, 2020-05, Vol.55 (5), p.689-690

2020

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Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy

Neurology, 2002-04, Vol.58 (7), p.1122-1124

2002

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Four‐vessel umbilical cord

Ultrasound in obstetrics & gynecology, 2011-11, Vol.38 (5), p.604-606

2011

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Acute encephalopathy in a patient with Dravet syndrome

Neuropediatrics, 2011-04, Vol.42 (2), p.78-81

2011

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P02.18: Early second‐trimester amniotic shelf—a common, transient, benign finding on early second‐trimester sonography

Ultrasound in obstetrics & gynecology, 2006-09, Vol.28 (4), p.526-527

2006

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Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures

Neurology, 2001-08, Vol.57 (4), p.703

2001

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A Nonsense Mutation of the Sodium Channel Gene SCN2A in a Patient with Intractable Epilepsy and Mental Decline

The Journal of neuroscience, 2004-03, Vol.24 (11), p.2690-2698

2004

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P04 .13: Evaluating STIC technology as a tool in training non‐expert sonographers to perform comprehensive fetal echocardiography

Ultrasound in obstetrics & gynecology, 2013-10, Vol.42 (s1), p.126-126

2013

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P04.13: Evaluating STIC technology as a tool in training non‐expert sonographers to perform comprehensive fetal echocardiography

Ultrasound in obstetrics & gynecology, 2013-10, Vol.42 (s1), p.126-126

2013

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P06.24: Omega shaped anomaly of the umbilical artery: a case series

Ultrasound in obstetrics & gynecology, 2011-10, Vol.38 (S1), p.190-190

2011

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Mutations of sodium channel α subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic–clonic seizures

Brain (London, England : 1878), 2003-03, Vol.126 (3), p.531-546

2003

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Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na +)-channel α1 subunit gene, SCN1A

Epilepsy research, 2002, Vol.48 (1), p.15-23

2002

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P09.04: Four‐vessel umbilical cord

Ultrasound in obstetrics & gynecology, 2011-10, Vol.38 (S1), p.200-200

2011

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OP33.05: The prenatal diagnosis of isolated varix of the fetal intra‐abdominal umbilical vein (VFIUV): iatrogenic prematurity is not obligatory

Ultrasound in obstetrics & gynecology, 2010-10, Vol.36 (S1), p.148-148

2010

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Pain Relief of Hysterosalpingography by Prior Uterine Cervical Application of Lidocaine/Prilocaine Cream

Fertility and sterility, 2005-09, Vol.84, p.S127-S128

2005

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A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures

Brain & development (Tokyo. 1979), 2005-09, Vol.27 (6), p.424-430

2005

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Nav1.1 predominantly localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in Nav1.1-deficient mice

Neuroscience research, 2007, Vol.58, p.S40-S40

2007

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Lack of anti-D in women at birth following antepartum immune globulin prophylaxis

European journal of obstetrics & gynecology and reproductive biology, 2003-03, Vol.107 (1), p.45-46

2003

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Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A

Epilepsy research, 2002-01, Vol.48 (1-2), p.15-23

2002

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De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsies

Neurology, 2009-09, Vol.73 (13), p.1046

2009

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A family of generalized epilepsy with febrile seizures plus type 2—a new missense mutation of SCN1A found in the pedigree of several patients with complex febrile seizures

Epilepsy research, 2005-02, Vol.63 (2), p.151-156

2005

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Na v 1.1 mutations cause febrile seizures associated with afebrile partial seizures

Neurology, 2001-08, Vol.57 (4), p.703-705

2001

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A missense mutation of the Na super(+) channel alpha sub(II) subunit gene Na sub(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

Proceedings of the National Academy of Sciences - PNAS, 2001-05, Vol.98 (11), p.6384-6389

2001

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A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

Proceedings of the National Academy of Sciences - PNAS, 2001-05, Vol.98 (11), p.6384-6389

2001

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De novo mutations of voltage-gated sodium channel α II gene SCN2A in intractable epilepsies

Intraoperative sonographic detection of ureteral jet during uncomplicated Cesarean delivery is feasible and safe

Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy

Four‐vessel umbilical cord

Acute encephalopathy in a patient with Dravet syndrome

P02.18: Early second‐trimester amniotic shelf—a common, transient, benign finding on early second‐trimester sonography

Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures

A Nonsense Mutation of the Sodium Channel Gene SCN2A in a Patient with Intractable Epilepsy and Mental Decline

P04 .13: Evaluating STIC technology as a tool in training non‐expert sonographers to perform comprehensive fetal echocardiography

P04.13: Evaluating STIC technology as a tool in training non‐expert sonographers to perform comprehensive fetal echocardiography

P06.24: Omega shaped anomaly of the umbilical artery: a case series

Mutations of sodium channel α subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic–clonic seizures

Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na +)-channel α1 subunit gene, SCN1A

P09.04: Four‐vessel umbilical cord

OP33.05: The prenatal diagnosis of isolated varix of the fetal intra‐abdominal umbilical vein (VFIUV): iatrogenic prematurity is not obligatory

Pain Relief of Hysterosalpingography by Prior Uterine Cervical Application of Lidocaine/Prilocaine Cream

A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures

Nav1.1 predominantly localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in Nav1.1-deficient mice

Lack of anti-D in women at birth following antepartum immune globulin prophylaxis

Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A

De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsies

A family of generalized epilepsy with febrile seizures plus type 2—a new missense mutation of SCN1A found in the pedigree of several patients with complex febrile seizures

Na v 1.1 mutations cause febrile seizures associated with afebrile partial seizures

A missense mutation of the Na super(+) channel alpha sub(II) subunit gene Na sub(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

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