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2 edition of Metabolism in myotonia atrophica found in the catalog.

Metabolism in myotonia atrophica

Sergius Morgulis

Metabolism in myotonia atrophica

report of a case

by Sergius Morgulis

  • 89 Want to read
  • 8 Currently reading

Published by American Medical Association in Chicago .
Written in English

    Subjects:
  • Myotonia atrophica.,
  • Metabolism.

  • Edition Notes

    Other titlesArchives of internal medicine.
    StatementSerguis Morgulis and Alexander Young ; with the assistance of J. K. Miller and E. Janecek.
    ContributionsYoung, Alexander, doctor., Miller, J. K., Janecek, E.
    The Physical Object
    Pagination7p. ;
    ID Numbers
    Open LibraryOL18595263M

    States of Altered Metabolism in Diseases of Muscle. In book: Advances in Enzymology and Related Areas of Molecular Biology, Volume 6, pp - nine patients with myotonia congenita and. Lippincott Journals Subscribers, use your username or email along with your password to log in., use your username or email along with your password to log in.

    Myotonia Myotonia Atrophica (Dystrophia Myotonica) THE pathologic aspects of the atrophic form of myotonia, a chronic hereditary disease of muscle, characterized by . Index Terms Starting With 'B' () › Baastrup's disease - see Kissing spine. Babesiosis B ICDCM Diagnosis Code B Billable.

    Full text of "A Text-book of the practice of medicine" See other formats. Full text of "The American journal of the medical sciences" See other formats.


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Metabolism in myotonia atrophica by Sergius Morgulis Download PDF EPUB FB2

Get this from a library. Myotonic dystrophy: disease mechanism, current management and therapeutic development.

[Masanori P Takahashi; Tsuyoshi Matsumura;] -- This book provides an essential overview combining both clinical and fundamental research advances Metabolism in myotonia atrophica book myotonic dystrophy. The pathomechanism of myotonic dystrophy has long been unclear, but in the.

In 2 patients with myotonia congenita, 2 with dystonia, muacutontm deformans and 1 with paralysis agitans, all syndromes representing pathologically increased muscular contraction, there was no defect of creatine and creatinine metabolism.

In 4 patients with myotonia atrophica there was a fall in creatinine excretion which appeared to be proportional to the reduction in muscle Cited by: Sergius Morgulis has written: 'Metabolism in myotonia atrophica' -- subject(s): Metabolism, Myotonia atrophica 'Fasting and undernutrition' -- subject(s): Fasting.

Myotonic dystrophy is part of a group of inherited disorders called muscular dystrophies. It is the most common form of muscular dystrophy that begins in adulthood. Myotonic dystrophy is characterized by progressive muscle wasting and weakness.

People with this disorder often have prolonged muscle contractions (myotonia) and are not able to relax certain. macrodontia, mental retardation, characteristic facies, short stature, and skeletal anomalies, see KBG syndrome.

macroglobulinemia of Waldenstrom, see Waldenström macroglobulinemia. macrothrombocytopenia, familial Bernard-Soulier type, see Bernard-Soulier syndrome. Macrozoospermia. macular degeneration, age-related, see Age-related macular.

Human muscular dystrophy is a condition of unknown etiology which produces progressive and severe dysfunction of symmetrical groups of skeletal muscle. Although its clinical manifestations and patterns of heredity have long been recognized, relatively little attention has been given the study Cited by: 5.

A similar condition may be seen in myotonia atrophica, in which the myotonia is accompanied by atrophy of the facial, sterno- mastoid, or quadriceps muscles, and is associated with endocrine dis- turbances.

It has also been reported by Krabbe,~ following an acute illness, presumably peripheral neuritis, and by Moore4 following severe by: 1. Brit J. Anaesth. (), 29, 35 THIOPENTONE IN DYSTROPHIA MYOTONICA BY TERENCE D.

BOURKE AND DAVID ZUCK Department of Anaesthesia, Chase Farm Hospital, Enfield action of creatine with adenosine triphosphate, (myotonia atrophica) is and this reaction is by: Metabolic studies made on 2 cases of progressive muscular dystrophy and on one case of myotonia atrophica showed normal Ca.

P and Mg balances, except that in one of the dystrophic patients there was a positive Ca balance even on a very reduced Ca intake. In a case of familial periodic paralysis there was a persistent negative P balance and considerable amounts of P Cited by: 9.

myotonica (myotonia atrophica), and many other indications, have led Siegrist to the conviction that cataract is a result of disturbance of the endocrine glands. There is muchto be said in favour of this hypothesis, and it is all well set out, with ample bibliography, in this work.

Forthis reason the book is a welcome addition to the. Neurologic Clinics, ISSN, Vol Issue 3, pp. - In medical contexts, a facies is a distinctive facial expression or appearance associated with a specific medical term comes from the Latin for "face".

As a fifth declension noun, facies can be both singular and lty: Medical genetics. However, it was not until ^, that both Batten and Gibb and Steinert formulated the syndrome of myotonia atrophica as an entity characterized by atrophy of certain muscle groups associated with active or passive myotonia, i.e., a tonic spasm of certain voluntary muscles with slow relaxation.

MYOTONIA ATROPHICA WITH TESTICULAR ATROPHY: URINARY EXCRETION OF INTERSTITIAL-CELL-STIMULATING (LUTEINIZING) HORMONE, ANDROGENS AND KETOSTEROIDS THE EIGHTH POSTGRADUATE ASSEMBLY IN ENDOCRINOLOGY AND METABOLISM.

J Clin Endocrinol Metab, Vol Issue 9, 1 SeptemberBOOK. This is a list of diseases starting with the letter "M". Muscle, which constitutes almost half of man's total body mass, is frequently the site of intrinsic disease and often is involved in systemic illness.

Of the intrinsic diseases of muscle, perhaps muscular dystrophy is the most common, afflicting several hundred thousand persons in the United States Cited by: 4. 20 From the late s to the mids, gelatin was the subject of many studies, and these were summarized in the book, Gelatin in Nutrition and Medicine, by Dr.

Gotthoffer. 21 In her article, "Why Broth is Beautiful," nutritionist Kaayla Daniel speculates that one of the reasons gelatin is so infrequently studied today, is due to a lack of. Define dystrophies. dystrophies synonyms, dystrophies pronunciation, dystrophies translation, English dictionary definition of dystrophies.

also dystrophia n. myotonia atrophica, myotonic dystrophy, After a well-written background section, a major portion of the book deals with the molecular approach to X-linked DMD, the most. Myotonic dystrophy (dystrophia myotonica, myotonia atrophica) is a chronic, slowly progressing, highly variable, inherited multisystemic disease.

It is an autosomal-dominant disease. It is characterized by wasting of the muscles (muscular dystrophy), cataracts, heart conduction defects, endocrine changes, and myotonia. ICDCM Book Edition. Chapters / Chapter 6 / GG Myotonia atrophica: Myotonic dystrophy: Proximal myotonic myopathy (PROMM) G Myotonia congenita: Acetazolamide responsive myotonia congenita: Dominant myotonia congenita [Thomsen disease] Myotonia levior: Recessive myotonia congenita [Becker disease] G Myotonic.

identity of myotonia congenita (thom-sen's disease), dystrophia myotonica (myotonia atrophica) and paramyotonia Maas, O; Paterson, A. S. The Journal of Nervous and Mental Disease. 91(1), January a disease or disorder that is inherited genetically.

a severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; .Obstetric anaesthesia in dystrophia myotonica.

29 consequences of myotonia atrophica (myotonic spasm after depolarizing muscle relaxants.