0
What else can I help you with?
Who discovered Saturn moons?
The first person to discover Saturn`s moons was Christian Huygens in 1655. The following moons discovered in order are: Titan Discovered:1655 Discovered by:Christian Huygens Iapetus Discovered:1671 Discovered by:Giovanni Cassini Rhea Discovered:1672 Discovered by:Giovanni Cassini Tethys Discovered:1684 Discovered by:Giovanni Cassini Dione Discovered:1684 Discovered by:Giovanni Cassini Enceladus Discovered:1789 Discovered by:William Herschel Mimas Discovered:1789 Discovered by:William Herschel Hyperion Discovered:1848 Discovered by:William Lassell Phoebe Discovered:1898 Discovered by:William Pickering Janus Discovered:1965-1966 Discovered by: Audouin Dollfus Epimetheus Discovered:1966 Discovered by:Richard Walker Helene Discovered:1980 Discovered by: Pierre Laques Telesto Discovered:1980 Discovered by:Bradford Smith Calypso Discovered:1980 Discovered by:Dan Pascu Prometheus Discovered:1980 Discovered by:Stewart Collins Pandora Discovered:1980 Discovered by:Stewart Collins Atlas Discovered:1980 Discovered by:Richard Terrile Pan Discovered:1981 Discovered by:Showalter Other astronomers:Kevin Beurile, Brett Gladman, Matthew Holman and others. If you want to see the rest, go to wikipedia.com to see the article Timeline discovery of solar system planets and their moons.
When were the rings on Neptune discovered?
they were discovered 17 days after the planet itself was discovered.
When was caesium discovered?
Caesium was discovered in 1860.
Where was the nickel discovered?
where was the element nickel discovered??
Who discovered ozone O3?
Ozone i.e. O3 was discovered by Charles Fabry. It was discovered in the year 1913.
What are the symptoms of Waldenstrom's macroglobulinemia?
Many individuals with WM have no symptoms of the disease. This is known as asymptomatic macroglobulinemia. When symptoms of WM are present, they may vary greatly
How can Waldenstrom's macroglobulinemia be prevented?
There is no known prevention for WM
Is waldenstroms hereditary?
Waldenstrom's macroglobulinemia is not considered hereditary, as most cases occur sporadically without a clear genetic link. However, some studies suggest a potential association with certain genetic predispositions, particularly in families with other lymphoproliferative disorders. While having a family history of related conditions may slightly increase risk, the majority of patients do not have a direct hereditary connection. Always consult a healthcare professional for personalized information regarding risk factors.
How is Waldenstrom's macroglobulinemia treated?
There also is no generally-accepted course of treatment for WM.
How prevalent is Waldenstrom's macroglobulinemia?
It is estimated that it may affect about five out of every 100,000 people
What demographic group gets Waldenstrom's macroglobulinemia?
WM most often affects males over the age of 65
What other names does Waldenstrom's macroglobulinemia have?
Other names that are sometimes used for WM include: lymphoplasmacytic lymphoma, lymphoplasmacytic leukemia,
MGUS - monoclonal gamapathy of undetermined sinifigance or WM Waldenstrom's Macroglobulinemia?
This isnt a meaningful question you might as well ask red or white?
What kind of disorder is Waldenstrom's macroglobulinemia?
All lymphomas other than Hodgkin's disease, including WM, are known collectively as non-Hodgkin's lymphomas.
When did Jack Gelber die?
Jack Gelber died on May 9, 2003, in New York City, New York, USA of Waldenstrom's macroglobulinemia.
What immunotherapy is used for Waldenstrom's macroglobulinemia?
Biological therapy or immunotherapy, with the potent, immune system protein interferon alpha, is used to relieve the symptoms of WM.
How is Waldenstrom's macroglobulinemia diagnosed?
Since many individuals with WM have no symptoms, the initial diagnosis may result from blood tests that are performed for some other purpose.
