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Nicholas M Allen

Showing results (21-30 of 56) with videos related to

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The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 21, 2010
Transcutaneous bilirubin--comparing the accuracy of BiliChek® and JM 103® in a regional postnatal unitYvonne M Qualter, Nicholas M Allen, John D Corcoran, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 15, 2020
Genetic potassium channel-associated epilepsies: Clinical review of the K<sub>v</sub> familyNicholas M Allen, Sarah Weckhuysen, Kathleen Gorman, et al.
Pediatric Neurology|November 26, 2011
"Stiff neonate" with mitochondrial DNA depletion and secondary neurotransmitter defectsMargaret M Moran, Nicholas M Allen, Eileen P Treacy, et al.
Neurology|December 3, 2015
Clinical Reasoning: Juvenile neurocognitive decline: A "snaky" diagnosisNicholas M Allen, Amre Shahwan, Cathy Madigan, et al.
Pediatrics|April 25, 2012
Excessive blinking and ataxia in a child with occult neuroblastoma and voltage-gated potassium channel antibodiesNicholas M Allen, Andrew McKeon, Declan J O'Rourke, et al.
American Journal of Medical Genetics. Part A|September 30, 2014
De novo interstitial deletion 2q14.1q22.1: is there a recognizable phenotype?Marie T Greally, Eve Robinson, Nicholas M Allen, et al.
Neurology|January 22, 2016
Salbutamol-responsive fetal acetylcholine receptor inactivation syndromeNicholas M Allen, Yael Hacohen, Jacqueline Palace, et al.
American Journal of Obstetrics and Gynecology|February 20, 2007
Expression and function of protease-activated receptor 4 in human myometriumNicholas M Allen, Margaret O'Brien, Anne M Friel, et al.
Pediatrics|April 4, 2018
Unusual Presentations of Dystrophinopathies in ChildhoodNicholas M Allen, Alice Ewer, Vasiliki Nakou, et al.
Stem Cell Research|April 18, 2023
Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.638C > T; p.Arg213Gln (NUIGi063-A, NUIGi063-B, NUIGi063-C) and 3 healthy controls (NUIGi064-A, NUIGi064-B, NUIGi064-C)Rachel Stewart, Cloe Gadoud, Janusz Krawczyk, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 21, 2010
Transcutaneous bilirubin--comparing the accuracy of BiliChek® and JM 103® in a regional postnatal unitYvonne M Qualter, Nicholas M Allen, John D Corcoran, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 15, 2020
Genetic potassium channel-associated epilepsies: Clinical review of the K<sub>v</sub> familyNicholas M Allen, Sarah Weckhuysen, Kathleen Gorman, et al.
Pediatric Neurology|November 26, 2011
"Stiff neonate" with mitochondrial DNA depletion and secondary neurotransmitter defectsMargaret M Moran, Nicholas M Allen, Eileen P Treacy, et al.
Neurology|December 3, 2015
Clinical Reasoning: Juvenile neurocognitive decline: A "snaky" diagnosisNicholas M Allen, Amre Shahwan, Cathy Madigan, et al.
Pediatrics|April 25, 2012
Excessive blinking and ataxia in a child with occult neuroblastoma and voltage-gated potassium channel antibodiesNicholas M Allen, Andrew McKeon, Declan J O'Rourke, et al.
American Journal of Medical Genetics. Part A|September 30, 2014
De novo interstitial deletion 2q14.1q22.1: is there a recognizable phenotype?Marie T Greally, Eve Robinson, Nicholas M Allen, et al.
Neurology|January 22, 2016
Salbutamol-responsive fetal acetylcholine receptor inactivation syndromeNicholas M Allen, Yael Hacohen, Jacqueline Palace, et al.
American Journal of Obstetrics and Gynecology|February 20, 2007
Expression and function of protease-activated receptor 4 in human myometriumNicholas M Allen, Margaret O'Brien, Anne M Friel, et al.
Pediatrics|April 4, 2018
Unusual Presentations of Dystrophinopathies in ChildhoodNicholas M Allen, Alice Ewer, Vasiliki Nakou, et al.
Stem Cell Research|April 18, 2023
Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.638C > T; p.Arg213Gln (NUIGi063-A, NUIGi063-B, NUIGi063-C) and 3 healthy controls (NUIGi064-A, NUIGi064-B, NUIGi064-C)Rachel Stewart, Cloe Gadoud, Janusz Krawczyk, et al.
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