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1 oeuvres 51 utilisateurs 12 critiques

A propos de l'auteur

Dr. Hiroshi Mitsumoto is the Director of the Eleanor and Lou Gehrig MDA/ALS Research Center and Wesley J. Howe Professor of Neurology at Columbia University. He received the Forbes H. Norris Award for Compassion and Love for Humanity in Research and Treatment in Patients with ALS from International afficher plus MND/ALS Symposium and International ALS Alliance in 1998. Dr. Mitsumoto has published widely on the subject. afficher moins

Œuvres de Hiroshi Mitsumoto

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Cette critique a été écrite dans le cadre des Critiques en avant-première de LibraryThing.
Dr Mitsumoto in his informative handbook collected articles from various experts surrounding any aspect of Lou Gehrig's disease, covering physical symptoms as well as emotional aspects, treatments and care. This book is a comprehensive reference handbook of value to patients, their families and care givers alike.
½
 
Signalé
RoyalScatterBrain | 11 autres critiques | Dec 31, 2012 |
Cette critique a été écrite dans le cadre des Critiques en avant-première de LibraryThing.
This is quite a meaty, informative book on ALS, written primarily for patients & families, although would be helpful for anyone seeking additional information about the disease itself &/or ways in managing it. Although for my purposes, it's more of a reference book that I & my family skim through as needed, it appears to be very well written for the lay person, yet technical enough to be very well validated. As a physical therapist myself, as well as the daughter of a parent currently battling ALS, I find this perhaps the single most valuable tool for referencing additional & up-to-date information concerning this disease. Very thorough & extremely helpful.… (plus d'informations)
½
 
Signalé
indygo88 | 11 autres critiques | May 22, 2010 |
Cette critique a été écrite dans le cadre des Critiques en avant-première de LibraryThing.
Perhaps the greatest challenge of writing a medical text is balancing the dissemination of information with accessibility. This book does an excellent job of walking this line. It manages to neither be too complex nor to be dumbed down to the point of uselessness. The book demands something the reader--but readers willing to put in the effort should be able to learn about ALS without a scientific background.

The book is targeted toward patients and their families and contains a wealth of information on everything from selecting wheelchairs to clinical features and prognosis. The book is fully updated with recent and accurate information. The book contains full references to other works and is fully cited for those looking to learn more.… (plus d'informations)
 
Signalé
Galorette | 11 autres critiques | Feb 21, 2010 |
Cette critique a été écrite dans le cadre des Critiques en avant-première de LibraryThing.
I found this book to be very helpful for anyone dealing with a loved one who has ALS - My Grandmother passed away with ALS and I would have loved to have had this resource to guide our family though the diagnosis and progression of ALS. Some area's are more technical than our needs, but their is information for eveyone in this one volume.

I would recommend this item be available when a patient is suspected of having ALS - the book is well written and has the answers to many of the questions we had.

I asked my Mother if she would like to review this book, and her thought were the same as mine. I very useful book for anyone dealing with people diagnosed with ALS.
… (plus d'informations)
 
Signalé
WCollett | 11 autres critiques | Nov 22, 2009 |

Statistiques

Œuvres
1
Membres
51
Popularité
#311,767
Évaluation
½ 4.5
Critiques
12
ISBN
15

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