Stories by SWNS on MSN
Baby’s wide eyes reveal syndrome so rare it has no name
Oska-Gray Valentine-Colquhoun, 20 months old, spent his first days in the NICU after being born in distress. He had to have ...
When she was 3 years old, Alana “Lani” Silverberg was eating a cookie when she started turning blue. Her mom, Sara, thought her daughter was choking and called 911. Lani was taken to Johns Hopkins ...
Doose syndrome is a rare seizure disorder that begins during early childhood. This condition is also called myoclonic astatic epilepsy and myoclonic atonic epilepsy. Doose syndrome is considered a ...
An Overview of the Neurological Mechanisms of Juvenile Myoclonic Epilepsy and Antiepileptic Drugs ()
Juvenile Myoclonic Epilepsy (JME) is a prevalent form of generalized epilepsy, predominantly affecting adolescents and young adults. It is characterized by myoclonic seizures, grand mal seizures, and ...
ABSTRACT: Juvenile Myoclonic Epilepsy (JME) is a prevalent form of generalized epilepsy, predominantly affecting adolescents and young adults. It is characterized by myoclonic seizures, grand mal ...
SEATTLE, Wash. -- Scientists at the Allen Institute have made a major breakthrough in research for people living with Dravet Syndrome, which is a rare and debilitating form of epilepsy that starts ...
I was diagnosed with juvenile myoclonic epilepsy (JME) at 15 years old after experiencing two tonic-clonic seizures in high school. What started as a typical morning quickly turned into a defining ...
If your doctor has suggested that you may have a myopathy, you likely have a lot of questions. There are many types of myopathies with different causes and outlooks. Myopathies are a class of diseases ...
Sleep myoclonus is involuntary, nonrhythmic muscle twitching that occurs either as a person falls asleep or during sleep. The movements include hiccups, starts, and jerks. Sleep myoclonus is not a ...
Objective To evaluate efficacy and safety of lacosamide (up to 12 mg/kg/day or 400 mg/day) as adjunctive treatment for uncontrolled primary generalised tonic-clonic seizures (PGTCS) in patients (≥4 ...
Voltage-gated sodium channels are essential for excitability of skeletal muscle fibres and neurons. An increasing number of disabling or fatal paediatric neurological disorders linked to mutations of ...
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