FMPM MOOCs - Hémochromatose- Pr. Z. Samlani
FMPM MOOCs.
FMPM MOOCs
Prions (Spongiform encephalopathy)
What is spongiform encephalopathy? Spongiform encephalopathy is a degenerative brain disease caused by the accumulation of misfolded prion proteins.
Osmosis
An Overview of Hereditary Haemorrhagic Telangiectasia (HHT) by Prof Claire Shovlin
An overview of Hereditary Haemorrhagic Telangiectasia (HHT) by VASCERN's HHT WG Chair, Prof Claire Shovlin. This Pill of Knowledge (PoK) is accessible to ...
VASCERN ERN Rare Vascular Diseases
Lambert-Eaton myasthenic syndrome - causes, symptoms, diagnosis, treatment, pathology
What is Lambert-Eaton myasthenic syndrome? Lambert-Eaton myasthenic syndrome is a rare autoimmune disease that attacks the peripheral nervous system, ...
Osmosis
Le sindromi ereditarie legate al cancro
In alcune famiglie il rischio di ammalarsi di tumore è più alto che nel resto della popolazione. Che cosa significa avere una predisposizione genetica a ...
IFOM
Gorlin syndrome
This is a lecture about the genetic condition Gorlin syndrome (nevoid basal cell carcinoma syndrome), designed for trainees and medical professionals. Lecture ...
Learn Medical Genetics
Cowden Syndrome and Cancer Genetic Testing at Ohio State
To learn more about cancer genetic testing or to schedule an appointment, visit https://wexnermedical.osu.edu/genetics or call 614-293-6694. Cowden ...
Ohio State Wexner Medical Center
What is Li-Fraumeni Syndrome? | Dana-Farber Cancer Institute
Judy Garber, MD, MPH, Director of the Center for Cancer Genetics and Prevention, describes Li-Fraumeni syndrome, a hereditary disorder that increases the ...
Dana-Farber Cancer Institute
Septic arthritis - causes, symptoms, diagnosis, treatment, pathology
What is septic arthritis? In septic arthritis there's joint inflammation, which can be caused by various bacterial infections which spread contiguously or ...
Osmosis
Introduction to Beckwith-Wiedemann Syndrome (BWS)
Beckwith-Wiedemann Syndrome (BWS) is a rare genetic disorder characterized by overgrowth. https://www.chop.edu/BWS 0:09 What is Beckwith-Wiedemann ...
The Children's Hospital of Philadelphia
Why Does Lynch Syndrome Occur in Families? | Dana-Farber Cancer Institute
Learn about our dedicated Lynch Syndrome Center - https://www.dana-farber.org/lynchsyndrome C. Richard Boland, MD, Professor of Medicine at the University ...
Dana-Farber Cancer Institute
Hereditary Haemorrhagic Telangiectasia from VASCERN HHT
An Introduction to Hereditary Haemorrhagic Telangiectasia (HHT) by the VASCERN HHT-WG is a video that introduces the HHT-WG and their expertise in this ...
VASCERN ERN Rare Vascular Diseases
Cowden Syndrome
Easy Dentistry by Dr Pranali Satpute
Amélie Taillon - Témoignage sur le syndrome de Cowden
Amélie Taillon - Témoignage sur le syndrome de Cowden. Référence: Regroupement québécois des maladies orphelines RQMO.
RQMOMalOrph
Alex's Story: PTEN Hamartoma Tumor Syndrome
Alex shares his story of living with PTEN hamartoma tumor syndrome and coming to Mass. Eye and Ear for treatment of his ears and hearing. Watch Alex's story ...
Mass. Eye and Ear
Peutz Jegher syndrome
Educational leacture Science
Dr. Felipe Ades - Síndrome de Li-Fraumeni e sua relação com o câncer de mama.
Whatsapp (11) 98335-4334 Para saber mais informações sobre câncer, tratamento, prevenção e bem estar visite http://drfelipeades.com/ Visite também nossa ...
Dr. Felipe Ades MD PhD
La gestione delle malattie rare al CEMAD
La Dott.ssa Annalisa Tortora (Specialista in Gastroenterologia) parla degli approcci e le metodologie per la gestione delle malattie rare al CEMAD Centro ...
CEMAD - Policlinico Universitario A. Gemelli IRCCS
HHT Center of Excellence | UPMC
A UPMC and University of Pittsburgh Schools of the Health Sciences clinical and academic partnership has earned international recognition as a premier center ...
UPMC
DIA 2019: The Li-Fraumeni Syndrome Association: Changing the Face of the Disease
Kathleen Higgins, Director of Community Outreach for the LFSAssociation, discusses Li-Fraumeni Syndrome, an inherited familial disposition to certain cancers, ...
DIA
Hereditary Cancer Syndromes
BRCA 1 and BRCA 2 mutations, Lynch syndrome, familial adenomatous polyposis (FAP), Li-fraumeni syndrome and Cowden syndrome are the most common ...
All Health TV
PTEN PSA
Zane's incredible #PTEN journey. Will you join us in making a difference for our #PTEN community? #Hereditarycancer #raredisease #PHTS #BRRS ...
PTEN Foundation
#Kankannyèz : Frappée par plusieurs tumeurs à l'âge de 13 ans !
Frappée en pleine adolescence par plusieurs tumeurs et par le syndrome de Peutz-Jeghers qui touche 1 enfant sur 200 000, Clara a su faire de ces moments ...
I Am Karibbean
Cowden's syndrome patient shares her experience
Amélie Taillon speaks about the disease that afflicts her, Cowden disease. (Pierre Obendrauf / MONTREAL GAZETTE)
Montreal Gazette
Parlons un peu sérieusement... du Syndrome de Lynch
Je m'appelle Karine, plus communément appelée Yusuradreams ou Yusu' sur Internet. Je suis atteinte du syndrome de Lynch et aujourd'hui je vous parle un ...
Yusura Dreams
Giornata Malattie Rare: sindromi dell’apparato digerente
Per la giornata delle malattie rare del 28 febbraio abbiamo sentito la Dott.ssa Vittoria Stigliano, responsabile Gastroenterologia ed Endoscopia Digestiva del ...
UfficioStampaIFO
MRCP PACES CONDITIONS: Neoplastic Syndromes
In this episode, we talk briefly about some neoplastic disorders that feature in the PACES examination: 1. MEN Syndrome 2. Von Hippel Lindau 3. Peutz Jeghers ...
MedStuffTalks
2015 06 19 Enfermedad de Rendu Osler
Enfermedad Rendu Osler.
Medicina Interna
Café-au-lait spots
This is a virtual blackboard outline of Café-au-lait spots found in conditions such as Neurofibromatosis Type 1 and McCune Albright Syndrome. I illustrate ...
Doctor O'Donovan
Bloom Syndrome
Find doctors and ongoing clinical trials - https://www.xpertdox.com/disease/description/Bloom%20Syndrome Bloom syndrome is a rare genetic disorder ...
XpertDox
What is FAMMM (familial atypical multiple mole and melanoma syndrome)?
Dr. Anil Rustgi discusses FAMMM (familial atypical multiple mole and melanoma syndrome). Join our online communities to begin receiving free continuing ...
MediCom Oncology
UCSF Radiology: PTEN Hamartoma Syndrome
Dr. Christopher Dowd, Interventional Radiologist, and Dr. Ilona Frieden, Pediatric Dermatologist, discuss diagnosing PTEN Hamartoma Syndrome using ...
UCSF Imaging
Warthin tumor - causes, symptoms, diagnosis, treatment, pathology
What is Warthin tumor? Warthin tumor, aka papillary cystadenoma lymphomatosum, is a type of benign tumor of the parotid gland. Find more videos at ...
Osmosis
Inflammatory Bowel Disease - Crohns and Ulcerative Colitits
http://armandoh.org/ https://www.facebook.com/ArmandoHasudungan Support me: http://www.patreon.com/armando Instagram: ...
Armando Hasudungan
Hypothalamic Hamartomas Research/Genetics of HH - Dr. Jack Kerrigan
by Jack Kerrigan, MD, Neurologist, Barrow Neurological Institute 2015 Hope For HH - Family Conference.
Hope For Hypothalamic Hamartomas
Poliposi familiare e sindrome di Lynch
Per la giornata delle malattie rare del 28 febbraio abbiamo sentito la Dott.ssa Lupe Sanchez, gastroenterologia del Regina Elena, sulla poliposi familiare e la ...
UfficioStampaIFO
Flow Technology door Peutz (incl. subtitles)
Meer informatie: https://www.peutz.nl/expertises/windtechnologie.
Peutz
Gorlin-Goltz Syndrome
A quick presentation and overview of the nevoid basal cell carcinoma syndrome with the help of a clinical case from the Contemporary Clinical Dentistry.
Professional Dental E-Class
O que é a síndrome de Melkersson Rosenthal ? ?
Este é um dos meus vídeos sobre uma ampla gama de recursos educacionais para garantir que informações vitais para médicos, pacientes e famílias estejam ...
Saúde
I "pacemaker" che regolano la digestione
Si è svolto a Firenze il VII Simposio Internazionale sulle Cellule Interstiziali di Cajal. Il Simposio è organizzato da Maria Simonetta Faussone-Pellegrini, ...
Medico e Paziente - MeP Edizioni
What is Klippel Trenaunay Syndrome? - Part 2
Go to: http://www.ktfoundation.org/ Together We Can Solve the Puzzle KT Foundation PO Box 205 Lakeview, NC 28350 What is KT? Klippel-Trenaunay ...
RedioVision
NEET MDS || SYNDROMES
neetmds2020 #oralpathomcqs.
mds and army dental exam preparation
