Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Detection of carriers of benign X-linked muscular dystrophy.

× No keyword cloud information.

10 in total

1. CREATINE KINASE LEVELS IN WOMEN WHO CARRY GENES FOR THREE TYPES OF MUSCULAR DYSTROPHY.

Authors: K M WILSON; K A EVANS; C O CARTER
Journal: Br Med J Date: 1965-03-20

2. ACTIVATION OF CREATINE PHOSPHOKINASE BY SULFHYDRYL COMPOUNDS IN NORMAL AND MUSCULAR DYSTROPHY SERA.

Authors: N C KAR; C M PEARSON
Journal: Proc Soc Exp Biol Med Date: 1965-03

3. A method for the estimation of serum creatine kinase and its use in comparing creatine kinase and aldolase activity in normal and pathological sera.

Authors: B P HUGHES
Journal: Clin Chim Acta Date: 1962-09 Impact factor: 3.786

4. Creatine and creatine kinase measurement.

Authors: M L TANZER; C GILVARG
Journal: J Biol Chem Date: 1959-12 Impact factor: 5.157

5. Muscular dystrophy in childhood; the genetic aspect; a field study in the Leeds region of clinical types and their inheritance.

Authors: H BLYTH; R J PUGH
Journal: Ann Hum Genet Date: 1959-04 Impact factor: 1.670

6. [Genetics of myopathy].

Authors: P E BECKER
Journal: Dtsch Z Nervenheilkd Date: 1955

7. X-linked pseudohypertrophic muscular dystrophy with a late onset and slow progression.

Authors: C C Mabry; I E Roeckel; R L Munich; D Robertson
Journal: N Engl J Med Date: 1965-11-11 Impact factor: 91.245

8. [A benign X-chromosomal hereditary muscular dystrophy. I. Examinations of symptom-carriers].

Authors: H W Rotthauwe; S Kowalewski
Journal: Humangenetik Date: 1966

9. Hereditary myopathies.

Authors: A E Emery
Journal: Clin Orthop Relat Res Date: 1964 Mar-Apr Impact factor: 4.176

10. Unusual type of benign x-linked muscular dystrophy.

Authors: A E Emery; F E Dreifuss
Journal: J Neurol Neurosurg Psychiatry Date: 1966-08 Impact factor: 10.154

10 in total

5 in total

1. The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.

Authors: R Skinner; A E Emery; A J Anderson; C Foxall
Journal: J Med Genet Date: 1975-06 Impact factor: 6.318

2. Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree.

Authors: G K Suthers; J I Manson; L M Stern; E A Haan; J C Mulley
Journal: J Med Genet Date: 1989-04 Impact factor: 6.318

3. [Biochemical, histological and clinical findings in a four-year-old female carrier of benign X-linked muscular dystrophy (Becker type)].

Authors: H Moser
Journal: Humangenetik Date: 1971

4. Freeze-fracture analysis of intramembrane particles of erythrocytes from normal, dystrophic, and carrier mice. A possible diagnostic tool for detection of carriers of human muscular dystrophy.

Authors: R R Shivers; B G Atkinson
Journal: Am J Pathol Date: 1979-01 Impact factor: 4.307

5. The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.

Authors: A J van Essen; A L Kneppers; A H van der Hout; H Scheffer; I B Ginjaar; L P ten Kate; G J van Ommen; C H Buys; E Bakker
Journal: J Med Genet Date: 1997-10 Impact factor: 6.318

5 in total