Two women, worlds apart, and a rare disease that could offer clues about ALS
Daily Magazine,
For more than 18 years, no one knew why Claudia Digregorio's muscles were slowly betraying her.
For more than 18 years, no one knew why Claudia Digregorio's muscles were slowly betraying her.
For more than 18 years, no one knew why Claudia Digregorio's muscles were slowly betraying her.
For more than 18 years, no one knew why Claudia Digregorio's muscles were slowly betraying her.
编辑推荐: 在一项对11名医学神秘患者的研究中,由美国国立卫生研究院(National Institutes of Health)和美国军装服务大学(USU)科学家领导的国际研究团队发现了一种新的、独特的肌萎缩侧索硬化症(ALS)。 美国国立卫生研究院和US…
/Maria Sbytova, stock.adobe.com Bethesda/Maryland Varianten in dem Gen SPTLC1 knnen die Produktion von Sphingolipiden in…
Claudia Digregorio tenía 5 años cuando empezó a tambalearse al caminar. Se cansaba.
Scientists have identified a new genetic form of amyotrophic lateral sclerosis in children, according to research published in…
(Reuters Health) - Scientists have identified four specific, dominant variants of the SPTLC1 gene in 11 children from seven…
La sclérose latérale amyotrophique (SLA) ou maladie de Charcot est une maladie neurodégénérative des neurones moteurs.
By sequencing the genomes of 11 individuals with a severe form of childhood amyotrophic lateral sclerosis (ALS), a team led by…
Six years ago, a teenager from Italy traveled to the U.S. in hopes of finding a diagnosis for her mysterious medical condition…
In a study of 11 medical-mystery patients, an international team of researchers led by scientists at the National Institutes of…
Some medical mysteries have become much easier to solve because of advanced genetic techniques that have enabled researchers to…
Some medical mysteries have become much easier to solve because of advanced genetic techniques that have enabled researchers to…
Some medical mysteries have become much easier to solve because of advanced genetic techniques that have enabled researchers to…
Some medical mysteries have become much easier to solve because of advanced genetic techniques that have enabled researchers to…
Six years ago, a teenager from Italy traveled to the U.S. in hopes of finding a diagnosis for her mysterious medical condition…
Исследователи выявили совершенно новую форму бокового амиотрофического склероза (БАС).
Researchers may have identified a potential treatment for the rare condition. (Image credit: Shutterstock) Six years ago, a…
Washington, June 1: In a study of 11 medical-mystery patients, an international team of researchers led by scientists at the…
NIH- and USU- led study links ALS to a fat manufacturing gene and maps out a genetic therapy In a study of 11 medical-mystery…
June 01, 2021 2 min read Source/Disclosures Disclosures: Healio Neurology could not confirm relevant financial disclosures for Bö…
Source: US Department of Health and Human Services – 2 News Release Tuesday, June 1, 2021 NIH- and USU- led study links ALS to…
After 11 patients presented with a mysterious neurological condition rendering them almost paralyzed, doctors have identified a…
In a study of 11 medical-mystery patients, an international team of researchers led by scientists at the National Institutes of…
Through an investigation of patients with a rare form of amyotrophic lateral sclerosis (ALS), researchers have discovered a new…
A previously unknown form of a severe and progressive neurodegenerative disease that usually affects older adults has been…
Childhood ALS linked to single-gene mutations. Credit: © SSilver - Depositphotos In a study of 11 medical-mystery patients, an…
NIH- and USU- led study links ALS to a fat manufacturing gene and maps out a genetic therapy In a study of 11 medical-mystery…
"ALS is a paralyzing and often fatal disease that usually affects middle-aged people.
In a study of 11 medical-mystery patients, an international team of researchers led by scientists at the National Institutes of…
Research Press Release Nature Medicine June 1, 2021 A specific class of rare mutations in the gene SPTLC1 — which encodes a key…
NIH- and USU- led study links ALS to a fat manufacturing gene and maps out a genetic therapy.
In a study of 11 medical-mystery patients, an international team of researchers has discovered a new and unique form of…
NIH- and USU- led study links ALS to a fat manufacturing gene and maps out a genetic therapy Credit: Courtesy of the NIH/NINDS.
NIH- and USU- led study links ALS to a fat manufacturing gene and maps out a genetic therapy Credit: Courtesy of the NIH/NINDS.
In a study of 11 medical-mystery patients, an international team of researchers led by scientists at the National Institutes of…
NIH researchers discovered a new form of ALS that begins in childhood. The study linked the disease to a gene called SPLTC1.
NIH researchers discovered a new form of ALS that begins in childhood. The study linked the disease to a gene called SPLTC1.
In a study of 11 medical-mystery patients, an international team of researchers led by scientists at the National Institutes of…