An evaluation of some carrier detection techniques in Duchenne muscular dystrophy

[1]  G. Nicholson,et al.  CARRIER DETECTION IN DUCHENNE MUSCULAR DYSTROPHY: ASSESSMENT OF THE EFFECT OF AGE ON DETECTION-RATE WITH SERUM-CREATINE-KINASE-ACTIVITY , 1979, The Lancet.

[2]  W. Engel,et al.  MYOGLOBINÆMIA IN DUCHENNE MUSCULAR DYSTROPHY PATIENTS AND CARRIERS: A NEW ADJUNCT TO CARRIER DETECTION , 1978, The Lancet.

[3]  M. Bobrow New ways to look at X inactivation , 1978, Nature.

[4]  H. Gruemer,et al.  Diminished cap formation in lymphocytes from patients and carriers of Duchenne muscular dystrophy. , 1977, Clinical chemistry.

[5]  R. Pennington,et al.  Effect of ouabain upon erythrocyte membrane adenosine triphosphatase in Duchenne muscular dystrophy , 1977, Journal of the Neurological Sciences.

[6]  J. Tukey Some thoughts on clinical trials, especially problems of multiplicity. , 1977, Science.

[7]  F. H. Tyler,et al.  Assessment of muscle strength in Duchenne muscular dystrophy , 1977, Neurology.

[8]  C. Roe,et al.  Pedigree testing in duchenne muscular dystrophy , 1977, Annals of neurology.

[9]  H. Soltan Echinocytes in families with Duchenne muscular dystrophy. , 1977, Journal of medical genetics.

[10]  A. Korczyn,et al.  Scanning electron microscope study of erythrocytes from patients with myopathy. , 1977, Israel journal of medical sciences.

[11]  W. Birchmeier,et al.  On the mechanism of ATP-induced shape changes in the human erythrocyte membranes: the role of ATP , 1977, The Journal of cell biology.

[12]  A. Engel,et al.  Failure of inactivation of Duchenne dystrophy X‐chromosome in one of female identical twins , 1977, Neurology.

[13]  A. Roses,et al.  Lactate dehydrogenase isoenzyme 5 in detecting carriers of Duchenne muscular dystrophy , 1977, Neurology.

[14]  A. Roses,et al.  Evaluation and detection of Duchenne's and Becker's muscular dystrophy carriers by manual muscle testing , 1977, Neurology.

[15]  W. Engel,et al.  Erythrocyte shape in Duchenne muscular dystrophy , 1976, Neurology.

[16]  V. Ionasescu,et al.  DETECTION of CARRIERS and GENETIC COUNSELING IN DUCHENNE MUSCULAR DYSTROPHY BY RIBOSOMAL PROTEIN SYNTHESIS , 1976, Acta neurologica Scandinavica.

[17]  K. Howells Structural changes of erythrocyte membranes in muscular dystrophy , 1976, Research in experimental medicine. Zeitschrift fur die gesamte experimentelle Medizin einschliesslich experimenteller Chirurgie.

[18]  G. Danieli,et al.  DUCHENNE CARRIER DETECTION , 1976, The Lancet.

[19]  G. Danieli,et al.  DUCHENNE CARRIER DETECTION , 1976, The Lancet.

[20]  M. Olarte,et al.  Biochemical abnormalities of erythrocyte membranes in Duchenne dystrophy. Adenosine triphosphatase and adenyl cyclase. , 1976, Archives of neurology.

[21]  K. Frankel,et al.  The pathology of the heart in progressive muscular dystrophy: epimyocardial fibrosis. , 1976, Human pathology.

[22]  A. Roses,et al.  Scanning electron microscopy studies in muscular dystrophy. , 1976, Archives of neurology.

[23]  A. Roses,et al.  Carrier detection in Duchenne muscular dystrophy. , 1976, The New England journal of medicine.

[24]  Michael E. Miller,et al.  Reduced deformability of erythrocyte membranes from patients with Duchenne muscular dystrophy , 1975, Nature.

[25]  A. K. van den Hoek,et al.  Studies on protein kinase activity and the binding of adenosine 3'5-monophosphate by membranes of hereditary spherocytosis erythrocytes. , 1975, Biochemical and biophysical research communications.

[26]  A. Emery,et al.  Erythrocyte deformation in duchenne muscular dystrophy. , 1975, British medical journal.

[27]  E. Lukasik Electrocardiographic studies in female carriers of Duchenne muscular dystrophy. , 1975, Journal of neurology.

[28]  A. Roses,et al.  Letter: Erythrocytes in human muscular dystrophy. , 1975, Science.

[29]  J. Graham-Pole,et al.  Immune status of children with and without severe infection during remission of malignant disease. , 1975, British medical journal.

[30]  G. Rodan,et al.  Abnormalities in membrane micro viscosity and ion transport in genetic muscular dystrophy , 1975, Nature.

[31]  A. Roses,et al.  Membrane protein kinase alteration in Duchenne muscular dystrophy , 1975, Nature.

[32]  H. Hansen,et al.  TREATMENT OF SMALL-CELL CARCINOMA OF BRONCHUS , 1975, The Lancet.

[33]  T. Miale,et al.  Erythrocytes in human muscular dystrophy. , 1975, Science.

[34]  J. L. Howland Abnormal potassium conductance associated with genetic muscular dystrophy , 1974, Nature.

[35]  F. Samaha,et al.  Serum pyruvate kinase in muscle disease and carrier states , 1974, Neurology.

[36]  J. L. Howland,et al.  Erythrocyte Deformation in Human Muscular Dystrophy , 1974, Science.

[37]  H. Moser,et al.  The manifesting carrier in Duchenne muscular dystrophy , 1974, Clinical genetics.

[38]  J. L. Howland,et al.  Erythrocytes from Animals with Genetic Muscular Dystrophy , 1973, Nature.

[39]  A. Afifi,et al.  A possible role for electron microscopy in detection of carriers of Duchenne type muscular dystrophy1 , 1973, Journal of neurology, neurosurgery, and psychiatry.

[40]  J. Eccleston,et al.  The direct interconversion of glucose and fructose in human skeletal muscle with special reference to childhood muscular dystrophy. , 1973, Clinical science.

[41]  J. Demos Platelet diphenoloxidases in Progressive Muscular Dystrophy (P.M.D.) , 1973, Clinical genetics.

[42]  E. Fisher,et al.  Ultrastructural changes in skeletal muscle of muscular dystrophy carriers. , 1972, Archives of pathology.

[43]  H. Brown,et al.  Further studies of membrane atpase activity in muscular dystrophy erythrocytes , 1972 .

[44]  A. Hudson,et al.  Fatty acid oxidation by skeletal muscle mitochondria in Duchenne muscular dystrophy. , 1972, Life sciences. Pt. 2: Biochemistry, general and molecular biology.

[45]  J. Walton,et al.  The detection of carriers of X-linked muscular dystrophy genes. A review of some methods studied in Newcastle upon Tyne. , 1971, Journal of the neurological sciences.

[46]  D. Wallach,et al.  Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. , 1971, Biochemistry.

[47]  S. Araki,et al.  Ouabain and erythrocyte-ghost adenosine triphosphatase. Effects in human muscular dystrophies. , 1971, Archives of neurology.

[48]  C. Pearson,et al.  Erythrocyte ghost adenosine triphosphatase (ATPase) in Duchenne dystrophy. , 1969, The Journal of laboratory and clinical medicine.

[49]  A. Emery Abnormalities of the Electrocardiogram in Female Carriers of Duchenne Muscular Dystrophy , 1969, British medical journal.

[50]  E. Merrill,et al.  Metabolic dependence of red cell deformability. , 1969, The Journal of clinical investigation.

[51]  G. Klassen,et al.  Adenosine triphosphatase and myopathy. , 1969, Science.

[52]  C. Suter,et al.  The use of serum lactate dehydrogenase isoenzymes in the diagnosis of muscle diseases , 1969, Neurology.

[53]  C. Slucka,et al.  The Electrocardiogram in Duchenne Progressive Muscular Dystrophy , 1968, Circulation.

[54]  O. Mann,et al.  Duchenne's Muscular Dystrophy: The Electrocardiogram in Female Relatives , 1968, The American journal of the medical sciences.

[55]  H. Brown,et al.  Erythrocyte Abnormality in Human Myopathy , 1967, Science.

[56]  W. Roberts,et al.  The distinctive electrocardiogram of Duchenne's progressive muscular dystrophy. An electrocardiographic-pathologic correlative study. , 1967, The American journal of medicine.

[57]  W. Askanas Identification of the agent responsible for the abnormal immunoelectrophoretic pattern of serum in Duchenne's progressive muscular dystrophy. , 1966, Life sciences.

[58]  J. Perloff,et al.  The Cardiomyopathy of Progressive Muscular Dystrophy , 1966, Circulation.

[59]  W. Askanas,et al.  The serum immunoelectrophoretic test in patients with Duchenne's progressive muscular dystrophy /preliminary report/ , 1966 .

[60]  A. Emery,et al.  MANIFESTATIONS IN CARRIERS OF X-LINKED MUSCULAR DYSTROPHY. , 1964, Lancet.

[61]  A. Emery Electrophoretic Pattern of Lactic Dehydrogenase in Carriers and Patients with Duchenne Muscular Dystrophy , 1964, Nature.

[62]  J. Pearce,et al.  Serum enzyme studies in muscle disease , 1964 .

[63]  W. A. Spencer,et al.  Muscle Testing: Part 2. Reliability in Clinical Use , 1961 .

[64]  Oliver H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[65]  T. Pearson,et al.  (Na++K+)-ATPase of Duchenne muscular dystrophy erythrocyte ghosts. , 1978, Life sciences.

[66]  G. Laudahn,et al.  [Diagnosis of female carriers of Duchenne's progressive muscular dystrophy using discriminative analysis of various serum enzyme activities]. , 1969, Klinische Wochenschrift.