Not exact matches
The researchers trialed their system on a female
patient who has locked - in
syndrome, a form of almost total paralysis caused
by brain lesions, at the Royal Hospital for Neuro - disability in London.
It is characterised
by inflammation and scaling of the skin, accompanied
by a greater risk of contracting some type of metabolic
syndrome, predisposing
patients to pathologies, such as obesity, diabetes or cardiovascular diseases.
The presence of antibodies to lymphadenopathy - associated retrovirus (LAV) was determined
by a radioimmunoprecipitation assay and
by an enzyme - linked immunosorbent solid assay of sera from Zairian
patients with the acquired immune deficiency
syndrome (AIDS) in 1983.
Immunoglobulin G (IgG) antibodies from
patients with the
syndrome, applied to bovine adrenal chromaffin cells, reduced the voltage - dependent calcium channel currents
by about 40 percent.
The illness was later renamed progressive supranuclear palsy (PSP) to describe the weakness or paralysis (palsy)
patients develop when brain areas that control eye movements are affected
by the
syndrome — which produces the classic symptom of motionless eyes described
by Dickens.
Compared with healthy controls,
patients with chronic fatigue
syndrome had less activation of the basal ganglia, as measured
by fMRI (functional magnetic resonance imaging).
The investigators obtained further evidence of the critical role of astroglial cells in Down
syndrome by implanting the skin - cell derived astroglial cells from Down
syndrome patients into mice.
George Daley of Harvard Medical School said on December 1 that he and his team have seen multiple
patients affected
by NEMO deficiency
syndrome, a disorder where an inherited faulty gene results in a weak immune system and leaves
patients prone to serious infections.
Zheng, together with Leah Boyer, then a researcher in Gage's lab and now director of Salk's Stem Cell Core, generated diseased neurons
by taking skin cells from
patients with Leigh
syndrome, reprogramming them into stem cells in culture and then coaxing them to develop into brain cells in a dish.
Use of the novel anticoagulant otamixaban did not reduce ischemic events compared with unfractionated heparin plus eptifibatide but increased bleeding among
patients with non-ST-segment elevation acute coronary
syndromes undergoing a percutaneous coronary intervention (PCI; procedures such as balloon angioplasty or stent placement used to open narrowed coronary arteries), according to a study published
by JAMA.
Importantly,
patients with mutations in a single copy of NKX2.1 often have Brain - Lung - Thyroid
Syndrome, which is characterized
by respiratory distress after birth and accompanied
by decreased surfactant protein expression.
Prader - Willi
syndrome (PWS) is a rare genetic disease characterized
by hyperphagia — a chronic feeling of hunger that, coupled with a metabolism that utilizes drastically fewer calories than normal, often leads to excessive eating and obesity in
patients with the disease.
To test this, the researchers did a side -
by - side comparison with cells isolated from elephants (n = 8), healthy humans (n = 10), and from
patients with Li - Fraumeni
Syndrome (n = 10).
Less p53 decreases the DNA damage response in
patients with Li - Fraumeni
Syndrome, and Schiffman's team wondered if more p53 could protect against cancer in elephants
by heightening the response to damage.
What's more, none of the
patients experienced macrophage activate
syndrome or cytokine release
syndrome, an infusion reaction observed in other gene therapy trials characterized
by fever, nausea, chills, hypotension or a rash.
The researchers, led
by Professor Sten Eirik W Jacobsen at the MRC Molecular Haematology Unit and the Weatherall Institute for Molecular Medicine at the University of Oxford, investigated malignant cells in the bone marrow of
patients with myelodysplastic
syndrome (MDS) and followed them over time.
Triheptanoin is an investigational medicine being developed
by Ultragenyx Pharmaceuticals for
patients with fatty - acid metabolism disorders and Glucose Transporter Type 1 Deficiency
Syndrome, which leads to epileptic seizures in young children.
Removal of the large intestine: Colectomy with ileorectal anastomosis, which removes the large intestine and attaches the small intestine to the rectum, is the primary treatment for
patients affected
by Lynch
syndrome who have colon cancer or precancerous colon polyps that can not be removed
by colonoscopy.
The international research team, led
by scientists at the University of Oxford and the Karolinska Institutet in Sweden, studied a group of
patients with myelodysplastic
syndromes — a malignant blood condition which frequently develops into acute myeloid leukaemia.
Dr Lucy Clark, lead author, Queen Mary University of London, UK, said: «We found that a self - help approach to a graded exercise program, guided
by a therapist, was safe and also helped to reduce fatigue for some people with chronic fatigue
syndrome, suggesting that GES might be useful as an initial treatment for
patients to help manage symptoms of chronic fatigue
syndrome.
Writing in a linked Comment, Dr Daniel J Clauw, Chronic Pain and Fatigue Research Centre, the University of Michigan, USA, says: «The finding that graded exercise therapy is effective even when exercise is not being witnessed and directly guided
by a physiotherapist is a substantial advance, since many
patients with chronic fatigue
syndrome and other functional impairment have difficulty getting to physiotherapy or do not have access to appropriately trained physiotherapists... In summary, findings from this pragmatic randomised controlled trial add to the evidence that straightforward, non-pharmacological therapies can be helpful in the management of symptoms such as fatigue in individuals with chronic fatigue
syndrome.
This mutation replicates the genetics of Coffin - Siris
syndrome, a disorder that some
patients with defects in the ARID1B gene have that is characterized
by speech and social development problems, intellectual disability, and delayed physical growth.
A new study led
by scientists at The Scripps Research Institute (TSRI) is giving researchers a first look at the early stages of brain development in
patients with Fragile X
syndrome, a disorder that causes mild to severe intellectual disability and is the most common genetic cause of autism spectrum disorder.
But scientists working on the deadly Middle East respiratory
syndrome (MERS) virus are puzzled
by two papers appearing in separate journals that not only tell the same story, but also are based on data from the very same
patient in Saudi Arabia.
In the case of the family examined
by the Brigham Genomic Medicine Program (BGMP), the primary
patient tested negative for the genetic mutations that cause Marfan
syndrome as well as all other mutations known to cause TAAD.
Dr. Siqueira said she and her colleagues are now investigating whether the problem was the result of an auto - immune disorder sparked
by one of the viruses that caused the immune system to attack nerve cells, similar to what occurs in Zika
patients who develop Guillain - Barré
Syndrome.
By comparing RNA sequencing with the Human Protein Atlas, we've also been able to identify new markers for the bile ducts that confirm the malformations that develop in
patients with Alagille
Syndrome.»
A new study led
by researchers at Sanford Burnham Prebys Medical Discovery Institute (SBP) identifies potential new therapeutic avenues for
patients with Alagille
syndrome.
Working at the University of California, Davis, the researchers created a new cellular model for studying Down
syndrome by taking skin cells from
patients with Down
syndrome and inducing them into a pluripotent state.
Mesenchymal stromal cells from
patients with myelodyplastic
syndrome display distinct functional alterations that are modulated
by lenalidomide.
«Kleefstra
syndrome is characterized
by mutations in EHMT1, and although these
patients had similar clinical symptoms to Kleefstra
syndrome, they didn't have the mutation.»
Our MDS center headed
by Dr Amit Verma is recognized as a national «center of excellence»
by the MDS Foundation and offers a variety of treatments and clinical trials for
patients with Myelodysplastic
syndromes.
Functional correction of T cells derived from
patients with the Wiskott - Aldrich
syndrome (WAS)
by transduction with an oncoretroviral vector encoding the WAS protein.
Plus, the grant will help them work with researchers led
by Doug Nordli, M.D., at the Lurie Children's Hospital at Northwestern University, which has a large clinical program for Dravet
syndrome and will look at heart rhythm activity during and after seizures in its
patients as part of the study.
The stem cells actually started out as skin cells donated
by patients with Dravet
syndrome, a severe form of childhood epilepsy — so they carry the genetic defect that causes that disease.
Prediction of short - and long - term outcomes
by troponin T levels in low - risk
patients evaluated for acute coronary
syndromes
«This study reinforces our previous research
by noting that the elective freezing of embryos is safer for all IVF
patients (ovulatory and anovulatory)
by reducing the risk of ovarian hyperstimulation
syndrome,» Legro said.
In
patients with diseases like irritable bowel
syndrome and Crohn's, gut microbiome is often less diverse, altered
by our low - plant - fiber Western diet and antibiotics.
For the trial, researchers enrolled 120 children from 2 to 18 years old with Dravet
syndrome, a rare genetic form of epilepsy that kills up to 20 percent of
patients by the time they are 20.
A recent study
by Lombardi et al. [1] describing a gamma - retrovirus infection in 68 of 101 chronic fatigue
syndrome (CFS)
patients was notable not only for its claim of a new viral aetiology of a hitherto controversial disease, but also for the fact that proviral DNA could be amplified from the peripheral blood mononuclear cells (PBMC) of 3.75 % (8/218) of the healthy controls.
Chronic Fatigue
Syndrome (CFS), described
by patients as «brain fog», and recently renamed
by the Institute of Medicine as «Systemic Exertion Intolerance Disease (SEID)», is a pertinent topic... -LSB-...]
Efficacy of individualised diets in
patients with irritable bowel syndrome: a randomised controlled trial Ather Ali, 1 Theresa R Weiss, 1 Douglas McKee, 2 Alisa Scherban, 1 Sumiya Khan, 1 Maxine R Fields, 1 Damian Apollo, 1 Wajahat Z Mehal1 Published in BMJ, Open Gastroenterology View Publication Abstract Background Patients with irritable bowel syndrome (IBS) are often placed on diets guided by food intolerance assays, although
patients with irritable bowel
syndrome: a randomised controlled trial Ather Ali, 1 Theresa R Weiss, 1 Douglas McKee, 2 Alisa Scherban, 1 Sumiya Khan, 1 Maxine R Fields, 1 Damian Apollo, 1 Wajahat Z Mehal1 Published in BMJ, Open Gastroenterology View Publication Abstract Background
Patients with irritable bowel syndrome (IBS) are often placed on diets guided by food intolerance assays, although
Patients with irritable bowel
syndrome (IBS) are often placed on diets guided
by food intolerance assays, although these...
Treating Irritable Bowel
Syndrome with a Food Elimination Diet Followed
by Food Challenge and Probiotics https://www.tandfonline.com/doi/abs/10.1080/07315724.2006.10719567 «These data demonstrate that identifying and appropriately addressing food sensitivity in IBS
patients not previously responding to standard therapy results in a sustained clinical response and impacts on overall well being and quality of life in this challenging entity.»
Case in point: I work with a functional med doc who, upon being asked
by an obese
patient with metabolic
syndrome whether she should drink a can of diet pop or regular pop (because she absolutely had to have just one a day), the doc strongly recommeded the regular pop.
Berberine improves insulin sensitivity
by inhibiting fat store and adjusting adipokines profile in human preadipocytes and metabolic
syndrome patients.
There are dietary regimens prescribed
by endocrinologists that go as low as 1000 calories a day, which when partnered with a prescribed mix of aerobic and strength exercises are aimed at treating diet - borne diseases like metabolic
syndrome and diabetes — and they are perfectly safe for
patients.
A
syndrome is usually associated with several clinically recognizable features: signs (observed
by a physician), symptoms (reported
by the
patient), and phenomena or characteristics; all of which often occur together.
A recent study showed that a new drug — developed
by GW Pharmaceuticals and made from cannabidiol, which is one of the main compounds found in cannabis — was able to significantly reduce seizures in
patients with Lennox - Gastaut
syndrome.
Vincent Wants to Sea (Unrated) Road flick about a man with Tourette's
Syndrome (Florian David Fitz) who runs away to Italy from a Bavarian rehabilitation center accompanied
by his obsessive - compulsive roommate (Johannes Allmayer) and an anorexic
patient (Karoline Herfurth) in order to fulfill his late mother's last request.
In fact, the nation's mental health professionals are reporting the rise of a phenomenon they're calling «Trump
Syndrome,» which is heightened anxiety among
patients caused
by Trump's rise to power.