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eBooks Maladies génétiques

Si vous aimez les titres Maladies génétiques, vous allez adorer cette sélection.
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  • Biologie des Croyances

    Comment affranchir la puissance de la conscience, de la matière et des miracles

    par Bruce Lipton, Carl Lemyre ...
    Traduit par Frédérick Letia, Annie J. Ollivier ...
    Cette édition 10e anniversaire du livre à succès de Bruce Lipton, Biologie des croyances, est une version mise à jour afin de renforcer la prémisse centrale du livre en y intégrant les plus récentes découvertes scientifiques, et l’on sait qu’elles furent très nombreuses depuis une dizaine d’années. Biologie des croyances est une œuvre révolutionnaire dans le domaine de la nouvelle biologie. ... En savoir plus

    13,99 €

  • The Cystic Fibrosis Passport

    par Dr Dominic A Fitzgerald ...
    Professor Dominic Fitzgerald is a paediatric respiratory and sleep specialist working at The Children's Hospital at Westmead in Sydney. For 15 years he has worked closely with infants and children with cystic fibrosis (CF), sharing the ups and downs of the family journey as they come to terms with caring for a child with CF. The Cystic Fibrosis Passport is designed as a practical manual for people ... En savoir plus

    5,65 €

  • Nobody's Listening to Me-If Only They Could C Me

    A Daughter's Battle With Sickle Cell

    par Iris Wright-Hart ...
    A Story of Pain, Power, and Unseen StrengthMena's voice echoes through hospital walls, family memories, and journal pages-pleading, protesting, educating, surviving. Living with Sickle Cell Disease (specifically Hemoglobin SC), she's faced more than just physical pain. She's fought to be heard by doctors, understood by loved ones, and seen as more than a diagnosis.Told through the eyes of a mother ... En savoir plus

    6,17 €

  • Huntington's disease

    Things you should know (Questions and Answers)

    par Rumi Michael Leigh ...
    Huntington's Disease: Things You Should Know (Questions and Answers) is an essential guide for anyone seeking a comprehensive understanding of Huntington's disease. This book is designed to provide clear, concise, and accurate information about this complex neurological condition. Whether you're a student, healthcare professional, or someone affected by Huntington's disease, this book will serve ... En savoir plus

    2,99 € ou Gratuit avec Kobo Plus

  • Friedreich Ataxia, A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions

    par Kenneth Kee ...
    Friedreich ataxia is a rare disease and the most frequent inherited ataxia.It is a degenerative disorder that mainly affects the nervous system, muscles and the heart.It is often linked with cardiomyopathy or diabetesThere is progressive ataxia (in-coordination of muscles), dysarthria, reduced proprioception, vibration sense and muscle weakness.The inheritance is autosomal recessive.CauseThe gene ... En savoir plus

    2,99 €

  • DNA Nation

    How the Internet of Genes is Changing your Life

    par Sergio Pistoi ...
    "An indispensable resource for understanding the complex world of over-the-counter genetic testing ... the impressive book explores territory that is both easy to understand and enlightening."--Kirkus Review"Highly important, life-changing and delightfully written...[Pistoi] is pulling the rug out from under many of our preconceptions...with continuous wit and humor. A book which indeed demands to ... En savoir plus

    3,99 € ou Gratuit avec Kobo Plus

  • Living with HHT

    Understanding and Managing Your Hereditary Hemorrhagic Telangiectasia

    par Sara Palmer ...
    Collection series A Johns Hopkins Press Health Book
    Everything you need to know about nosebleeds, arteriovenous malformations, and other symptoms of HHT.Hereditary Hemorrhagic Telangiectasia (HHT) is a rare genetic disorder that causes blood vessel abnormalities in the nose, skin, gastrointestinal tract, lungs, brain, and liver. Nosebleeds are the most common symptom of HHT, but abnormal vessels in other organs, if they are not diagnosed and ... En savoir plus

    23,89 €

  • Patient 1

    Forgetting and Finding Myself

    par Charlotte Raven, Dr Edward Wild ...
    'Searingly honest and important' RACHEL CLARKEHonest, intelligent and unsentimental, Patient 1 is a startling self-portrait written with wit and vulnerability, and a unique testament to the power of hope in the face of illness.Charlotte Raven had never heard of Huntington's Disease when, in her mid-thirties, she discovered that her father was suffering from the illness. Life for her and her young ... En savoir plus

    12,99 €

  • Thalassemia, A Simple Guide To The Condition, Treatment And Related Conditions

    par Kenneth Kee ...
    Thalassemia is an inherited disorder of the Red blood cellsIt produces an abnormal Hemoglobin which makes the patient unwellThe patients usually inherit the disease from his parentsIf both parents are affected, having thalassemia major child is 25 per centThere are 2 types of Thalassemia:Thalassemia major which is a serious severe form of anemiaThalassemia minor in a person who has received only ... En savoir plus

    2,99 €

  • Онкологія без паніки

    Як попереджають, виявляють і лікують рак

    par Ілона Свєженцева ...
    Саме лише слово «онкологія» нас лякає. Про цей спектр хвороб важко говорити, хочеться лише заплющити очі й удати, що раку не існує. Втім ігнорування не допомагає: онкологія була з нами ще задовго до нашого розуміння, як з нею боротися.Дослідниця й науковиця Ілона Свєженцева у своїй книжці просто та виважено розповідає про природу раку. Авторка пояснює, як відстежити перші ознаки хвороби, які є ... En savoir plus

    4,99 €

  • NATURAL REMEDIES FOR HEMOCHROMATOSIS

    Discover Natural Remedies For Reducing Iron Absorption And Managing Hemochromatosis

    par Maya Walker ...
    Hemochromatosis (hе-mое-krое-muh- TOE-ѕіѕ) саuѕеѕ уоur body to аbѕоrb tоо muсh іrоn frоm thе food you еаt. Exсеѕѕ іrоn іѕ ѕtоrеd іn уоur organs, еѕресіаllу уоur lіvеr, hеаrt and pancreas. Tоо muсh іrоn саn lеаd tо life-threatening conditions, ѕuсh аѕ lіvеr dіѕеаѕе, hеаrt problems аnd diabetes. The genes thаt саuѕе hemochromatosis аrе іnhеrіtеd, but оnlу a mіnоrіtу оf реорlе whо hаvе thе gеnеѕ ever ... En savoir plus

    4,41 € ou Gratuit avec Kobo Plus

  • Introduction to Viral Genetic Engineering

    par Edenilson Brandl ...
    Welcome to the world of "Introduction to Viral Genetic Engineering." In the pages that follow, we embark on a journey through the intricate landscape of genetic manipulation, where the tiniest of entities—viruses—become tools for profound scientific exploration, medical advancement, and, inevitably, ethical contemplation.The marvels of modern biotechnology have granted us the ability to peer into ... En savoir plus

    0,99 € ou Gratuit avec Kobo Plus

  • The Biogenealogy Sourcebook

    Healing the Body by Resolving Traumas of the Past

    par Christian Flèche ...
    A practical guide to the correspondence between emotion, organ systems, and disease• Identifies what emotional shocks will engender illnesses specific to a certain part of the body• Shows how illness is an ally that enables individuals to restore balance to their healthBiogenealogy is a comprehensive new vision of health that takes the mind-body connection one step further by identifying and ... En savoir plus

    14,05 €

  • Understanding sickle cell Anemia And it's natural management Strategies

    par Isaac Okondi Yohanna ...
    This eBook it's a comprehensive guide that talk about the genetic mutation of red blood cells in the body of a sickle cell patient and a Step by steps guide on how to manage the disease Naturally without the frequent use of modern day medication. The Ebook is very important for Caregiver, doctors, Nurses, Sickle cell Anemia patient and everyone as a whole. ... En savoir plus

    2,64 € ou Gratuit avec Kobo Plus

  • How To Become A Genealogy Expert

    par arther d rog ...
    Discover your ancestors' facts and riddles with a straightforward genealogical method.Finding a bigger familial historical picture, protecting the past for future generations, and storytelling are some of the main motivations for family history research. By developing an awareness of genealogy and the variables, activities, and challenges associated with the investigation, Practical Genealogy ... En savoir plus

    8,99 €

  • Der Mann mit dem Herzen aus Papier

    par Angelo Lorello ...
    Das sensationelle Story-Event signiert von Angelo Lorello Die Schwierigkeiten eines Kindes namens Christian, das in Alaska mit einer schrecklichen Herzkrankheit geboren wurde, für die es in seinem Land keine Operation, die ihn retten könnte, gibt, wenn nicht die, die von einem Team von Herzchirurgen in Spanien durchgeführt wird. Diesen Eingriff kann sich die Familie jedoch nicht leisten.... Eine ... En savoir plus

    9,99 €

  • Mommy, Please Don't Listen To Them

    A little girl's story about her fight for life

    par Denise F. Loewen ...
    Little Trina had health challenges from the start and over the course of her 27 short years their source seemed to mystify professionals from all branches of medicine. In Mommy, Please Don’t Listen to Them we are taken on a roller coaster ride that traverses the emotional ups and downs that shaped the lives of little Trina and her devoted family. Through Trina the author learned that when she ... En savoir plus

    2,05 €

  • Stop la chute de cheveux

    par Nazeem Nour ...
    Basé sur plusieurs années de recherches, ce livre électronique va vous montrer ce qu'il faut exactement faire pour arrêter la chute de vos cheveux et plus tard faire repousser vos cheveux. La méthode sur laquelle se base ce livre est naturelle, sans produit chimique quelconque. C'est une méthode basée sur votre mode de vie et c'est le programme anti-chute de cheveux le plus complet qui existe ... En savoir plus

    4,38 €

  • Vampiro in pigiama

    par Mathias Malzieu ...
    Traduit par Cinzia Poli ...
    Mathias Malzieu ha sempre sognato di essere un supereroe ma, scopre, anche i supereroi si ammalano. E spesso in maniera grave, al punto da ricorrere a un trapianto, proprio come accade a Mathias. Con la stessa leggerezza e ironia di Jack e Tom Cloudman, gli eroi dei suoi romanzi precedenti, l’autore narra in prima persona le cure mediche ricevute, le degenze negli ospedali, ma soprattutto mette a ... En savoir plus

    6,99 €

  • La trisomie 21

    Perspective historique sur son diagnostic et sa compréhension

    par Jean-Adolphe Rondal ...
    Bilan historique et génétique du syndrome de Down.La trisomie 21, habituellement nommée syndrome de Down, mais qui en toute équité historique devrait s’appeler syndrome de Seguin-Down-Lejeune, est le mieux connu et un des plus fréquents syndromes génétiques congénitaux du handicap cognitif. Il touche plus de 500.000 personnes en Europe seulement. L’incidence est supérieure à celle de la fibrose ... En savoir plus

    19,99 €

  • Cadeiras de rodas nunca mais

    Uma experiência cura da doença rara Porfiria Aguda Intermitente

    par Helena Lopes ...
    A autora conta sua experiência com a manifestação de uma doença rara do metabolismo (Porfiria Aguda Intermitente - PAI) que a levou à tetraparesia e a quase morte. Ela descreve com detalhes o agravamento da doença, as dificuldades médicas para a compreensão da enfermidade, o tempo até o diagnóstico e o andamento de sua recuperação física. Além de uma breve explicação a respeito do que as pesquisas ... En savoir plus

    2,49 € ou Gratuit avec Kobo Plus

  • The DNA Restart

    Unlock Your Personal Genetic Code to Eat for Your Genes, Lose Weight, and Reverse Aging

    par Sharon Moalem ...
    A practical guide to tailoring your diet to your genes, based on groundbreaking research on genetics, nutrition, and longevity—featuring at-home exercises like TikTok’s viral saltine cracker test!“Packed with fascinating information about the links between genes, food, and health.”—Stephen Le, PhD, author of 100 Million Years of FoodTake a bite of a cracker. As you chew, notice how long it takes ... En savoir plus

    8,02 €

  • Understanding Fragile X Syndrome

    A Guide for Families and Professionals

    par David Aldridge, Isabel Fernández Carvajal ...
    Collection series JKP Essentials
    Fragile X syndrome is one of the main causes of child developmental delay and autism spectrum disorders. A premutated form of the same gene is also the basis for neurological disabilities in adults. This book breaks down the complex science of this genetic disorder and provides the facts and advice that every bewildered parent or professional needs to support individuals with Fragile X syndrome ... En savoir plus

    16,57 €

  • Memory Matters: Your Complete Guide to a Healthy Brain

    par Susan Zeppieri ...
    An evidence-informed guide to nutrition and lifestyle factors that support brain health.Cognitive changes are a common concern as we age, and many people are interested in understanding how diet, nutrients, and daily habits may influence long-term brain health. This book provides a clear, balanced overview of current research on vitamins, minerals, and lifestyle factors commonly discussed in ... En savoir plus

    19,99 €