Hereditary Defect of Cobalamin Metabolism (CblGMutation) Presenting as a Neurologic Disorder in Adulthood

1988 ◽  
Vol 318 (26) ◽  
pp. 1738-1741 ◽  
Author(s):  
Ralph Carmel ◽  
David Watkins ◽  
Stephen I. Goodman ◽  
David S. Rosenblatt
2019 ◽  
Vol 130 (8) ◽  
pp. e145
Author(s):  
J. Motte ◽  
J. Kneiphof ◽  
K. Straßburger-Krogias ◽  
A.L. Fisse ◽  
L. Kappos ◽  
...  

1996 ◽  
Vol 60 (1) ◽  
pp. 107-108 ◽  
Author(s):  
R Gold ◽  
U Bogdahn ◽  
L Kappos ◽  
K V Toyka ◽  
E R Baumgartner ◽  
...  

2021 ◽  
pp. 153575972199832
Author(s):  
Karnig Kazazian ◽  
Marissa Kellogg ◽  
Nora Wong ◽  
Krista Eschbach ◽  
Raquel Farias Moeller ◽  
...  

New-onset refractory status epilepticus (NORSE) is a rare clinical presentation of refractory status epilepticus (RSE) that occurs in people without active epilepsy or preexisting neurologic disorder. Febrile infection-related epilepsy syndrome (FIRES) is a subcategory of NORSE. New-onset refractory status epilepticus/FIRES are becoming increasingly recognized; however, information pertaining to disease course, clinical outcomes, and survivorship remains limited, and mortality and morbidity are variable, but often high. The objective of the NORSE/FIRES Family Registry is to (1) provide an easily accessible and internationally available multilingual registry into which survivors or NORSE/FIRES surrogates or family members of people affected by NORSE/FIRES or their physicians can enter data in a systematic and rigorous research study from anywhere in the world where internet is available; and (2) to examine past medical history, outcomes, and quality of life for people affected by NORSE/FIRES.


1985 ◽  
Vol 60 (3) ◽  
pp. 211
Author(s):  
David G. Cogan
Keyword(s):  

2015 ◽  
Vol 2015 ◽  
pp. 1-3
Author(s):  
Christian Grønhøj Larsen ◽  
Mette Gyldenløve ◽  
Aia Elise Jønch ◽  
Birgitte Charabi ◽  
Zeynep Tümer

Idiopathic facial palsy (IFP), also known as Bell’s palsy, is a common neurologic disorder, but recurrent and familial forms are rare. This case series presents a three-generation family with idiopathic facial palsy. The mode of inheritance of IFP has previously been suggested as autosomal dominant with low or variable penetrance, but the present family indicates an autosomal dominant trait with high or complete penetrance. Chromosome microarray studies did not reveal a pathogenic copy number variation, which could enable identification of a candidate gene.


1976 ◽  
Vol 2 (2) ◽  
pp. 107-111 ◽  
Author(s):  
Yoshitaka Nagai ◽  
Takashi Momoi ◽  
Masaki Saito ◽  
Eizo Mitsuzawa ◽  
Sugishi Ohtani

1976 ◽  
Vol 10 (10) ◽  
pp. 900-900
Author(s):  
A Niederwieser ◽  
A Matasović ◽  
P Tippett ◽  
D M Danks ◽  
A Prader

1976 ◽  
Vol 34 (3) ◽  
pp. 277-283 ◽  
Author(s):  
Huntington F. Willard ◽  
Lalit M. Ambani ◽  
Anita C. Hart ◽  
Maurice J. Mahoney ◽  
Leon E. Rosenberg

2018 ◽  
Vol 38 (05) ◽  
pp. 539-547 ◽  
Author(s):  
Neil Vaishnav ◽  
Winston Chiong

AbstractThe doctrine of informed consent sits at the intersection of law, ethics, and neuroscience, posing unique challenges for human subject research involving neurological patients. These challenges are compounded by the variegated nature of both neurological injury and the law governing research consent. This article provides a framework for investigators likely to encounter subjects with some degree of neurological impairment, whose capacity to consent requires scrupulous assessment prior to enrollment in research trials. We consider several researches and disease contexts—from emergency epilepsy research to long-term dementia research—and clarify the ethical and legal principles governing consent for participation in each. We additionally explore empirical research on consent capacity and survey several areas of emerging ethical import that will require the attention of investigators in decades to come.


2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Abdulrahman M El-Sayed ◽  
Craig Hadley ◽  
Fasil Tessema ◽  
Ayelew Tegegn ◽  
John A Cowan ◽  
...  

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