rarekidneystones.org
Cystinuria - Rare Kidney Stone Consortium
http://www.rarekidneystones.org/cystinuria
David Goldfarb, MD. New York University, New York, NY and Lenox Hill Hospital, New York, NY. Join the Cystinuria Registry. The International Cystinuria Registry. Is now operational. Participation of patients will help physicians and scientists learn more about this rare disease, and help design new treatments. To learn more about the Cystinuria registry at New York University, please send an e-mail to cystinuria@nyumc.org or visit the official registry site. At New York University. International Cystinur...
cystinurie.com
5. Néphrolithotomie percutanée - CYSTINURIE // AIRG-France // Association pour l'Information et la Recherche sur les maladies Rénales Génétiques
http://www.cystinurie.com/la-maladie/6-nephrolithotomie-percutanee
Rechercher dans ce site. Vidéos journée cystinurie 2014. Vidéos journée cystinurie 2016. Par le Professeur Eric Lechevallier. Hôpital de la Conception, Marseille. Près de 50% des calculs urinaires peuvent nécessiter un traitement urologique. Dix pour cent des calculs qui sont traités le sont par une chirurgie percutanée. La chirurgie percutanée pour calcul rénal dite néphrolithotomie percutanée (NLPC) a été introduite en France en 1983. Le point de ponction est situé dans le dos. Le site de ponction ...
cystinurie.com
Conseils administratifs - CYSTINURIE // AIRG-France // Association pour l'Information et la Recherche sur les maladies Rénales Génétiques
http://www.cystinurie.com/conseils-administratifs
Rechercher dans ce site. Vidéos journée cystinurie 2014. Vidéos journée cystinurie 2016. Affection Longue Durée (ALD). Lors de la réalisation de votre protocole de soins avec votre médecin traitant pour une demande de reconnaissance en ALD (100%), indiquez à votre médecin de cocher la case "ALD 30 Liste". En effet, la Cystinurie est reconnue au titre des maladies métaboliques héréditaires comme le Ministre de la Santé l'avait précisé lors d'une question à l'Assemblée Nationale :. Si vous Néphrologue vous...
shakesandstones.blogspot.com
shakesandstones: Follow up wrap
http://shakesandstones.blogspot.com/2014/08/follow-up-wrap.html
Friday, August 15, 2014. However, although I would have to classify the trip as a success I still feel a little disappointed. Allow me to elaborate. This is my second evaluation. When I had the first one the results were nothing short of spectacular. Although they still demonstrated a "severe neuropathy", the improvement was marked and I felt a great deal better for it. Until next time, stay well:). August 15, 2014 at 9:00 PM. Eddie Nash here. It is always good to hear from you sir! Autologous Stem Cell ...
metabolic-disorders.blueprintgenetics.com
Genetic testing for inborn error of metabolism
http://metabolic-disorders.blueprintgenetics.com/panels/comprehensive-metabolism-panel
Blueprint Genetics - Metabolic Disorders. Ear Nose and Throat. Whole Genome Del/Dup (CNV). Our Sequence Analysis is based on a proprietary targeted sequencing method OS-Seq and offers panels targeted for genes associated with certain phenotypes. A standard way to analyze NGS data for finding the genetic cause for Mendelian disorders. Results in 21 days. Results in 3-4 weeks. We do not offer a maternal cell contamination (MCC) test at the moment. We offer prenatal testing only for cases where the ...Click...
shakesandstones.blogspot.com
shakesandstones: CIDP
http://shakesandstones.blogspot.com/p/cidp.html
CIDP can occur at any age and in both sexes, but is more common in men than women. Symptoms include tingling, numbness or altered feeling which often begins in the feet and hands, weakness of the arms and legs, fatigue and aching pain in the muscles. July 23, 2015 at 5:47 PM. Very nice post, impressive. its quite different from other posts. Thanks for sharing. Subscribe to: Posts (Atom). Autologous Stem Cell Transplant. Get your RSS here. International Essential Tremor Foundation. So, Why is it so?
shakesandstones.blogspot.com
shakesandstones: March 2014
http://shakesandstones.blogspot.com/2014_03_01_archive.html
Sunday, March 23, 2014. MS societies - Why so anti HSCT? It is a question that has puzzled many HSCT advocates, both inside and outside of the medical and patient community. To those of us that have understood the process and talked to people who have gone through the procedure and benefitted from it can't understand. Myself included. And why should the MS societies point people in the right direction? So why have MS societies and organisations been so anti HSCT? Anyway here are my reasons/theories:-.
shakesandstones.blogspot.com
shakesandstones: My Medical History
http://shakesandstones.blogspot.com/p/medical-history.html
Well, the gods didn't like it so one week later I had my first (of many) trips to the hospital. I hear you ask, “Why did you need to go to hospital? 8221; I had a kidney stone. The first of three I had that year. I was diagnosed with a condition known as cystinuria, which means I have to battle kidney stones regularly. Sometimes I won, mostly I lost. I also changed my nephrologist (Kidney specialist) completely. I also took time to work on my mental health and let myself know that what I had really did s...
shakesandstones.blogspot.com
shakesandstones: Two years
http://shakesandstones.blogspot.com/2014/04/two-years.html
Thursday, April 10, 2014. I am pinching myself. It has now been two years since I was in Chicago having my stem cells infused back into me. Ironically, the day seemed a bit like a non-event. After all the drugs and chemotherapy they put into me over my three week hospital stay the stem cell infusion seemed like just another hospital day. Until next time, stay well:). April 10, 2014 at 8:56 PM. So happy to see the updates that Wendys TOUR GUIDE posts! April 11, 2014 at 12:03 PM. What a great process!
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