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Lancet (London, England)
|
June 20, 1981
Human fibroblast interferon does not induce chromosomal abnormalities
C R Bartram, W Mortier, A Schmidt
Humangenetik
|
January 1, 1972
[New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias]
H W Rotthauwe, W Mortier, H Beyer
Humangenetik
|
January 1, 1975
[Centronuclear myopathy with autosomal dominant inheritance(author's transl)]
W Mortier, E Michaelis, J Becker, et al.
Muscle & Nerve
|
January 1, 1986
Screening for Duchenne muscular dystrophy: an improved screening test for creatine kinase and its application in an infant screening program
G Scheuerbrandt, A Lundin, T Lövgren, et al.
Der Anaesthesist
|
May 2, 2000
[Anesthetic complications. The incidence of severe anesthetic complications in patients and families with progressive muscular dystrophy of the Duchenne and Becker types]
E Breucking, P Reimnitz, U Schara, et al.
Der Anaesthesist
|
October 1, 1993
[Anesthesia and intensive therapy for a patient with mitochondrial myopathy]
E Breucking, W Mortier, R Lampert, et al.
Advances in Experimental Medicine and Biology
|
May 23, 1998
The genetic basis of myoadenylate deaminase deficiency is heterogeneous
E Rötzer, W Mortier, H Reichmann, et al.
Monatsschrift Fur Kinderheilkunde
|
October 1, 1977
[Are too many infants diagnosed as neurologically damaged? Comment on the early diagnosis and therapy of cerebral palsy]
G A Von Harnack, W Mortier, E Schmidt
Neuropediatrics
|
October 1, 1993
Subtotal aplasia of myelinated nerve fibers in the sural nerve
J M Schröder, G Heide, V Ramaekers, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
January 1, 1984
[Longtime care of spina bifida patients. Therapy and prognosis in the last 20 years]
H H Kramer, W Mortier, R Pothmann, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 61) with videos related to
Sort By:
Page
of 7
Lancet (London, England)
|
June 20, 1981
Human fibroblast interferon does not induce chromosomal abnormalities
C R Bartram, W Mortier, A Schmidt
Humangenetik
|
January 1, 1972
[New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias]
H W Rotthauwe, W Mortier, H Beyer
Humangenetik
|
January 1, 1975
[Centronuclear myopathy with autosomal dominant inheritance(author's transl)]
W Mortier, E Michaelis, J Becker, et al.
Muscle & Nerve
|
January 1, 1986
Screening for Duchenne muscular dystrophy: an improved screening test for creatine kinase and its application in an infant screening program
G Scheuerbrandt, A Lundin, T Lövgren, et al.
Der Anaesthesist
|
May 2, 2000
[Anesthetic complications. The incidence of severe anesthetic complications in patients and families with progressive muscular dystrophy of the Duchenne and Becker types]
E Breucking, P Reimnitz, U Schara, et al.
Der Anaesthesist
|
October 1, 1993
[Anesthesia and intensive therapy for a patient with mitochondrial myopathy]
E Breucking, W Mortier, R Lampert, et al.
Advances in Experimental Medicine and Biology
|
May 23, 1998
The genetic basis of myoadenylate deaminase deficiency is heterogeneous
E Rötzer, W Mortier, H Reichmann, et al.
Monatsschrift Fur Kinderheilkunde
|
October 1, 1977
[Are too many infants diagnosed as neurologically damaged? Comment on the early diagnosis and therapy of cerebral palsy]
G A Von Harnack, W Mortier, E Schmidt
Neuropediatrics
|
October 1, 1993
Subtotal aplasia of myelinated nerve fibers in the sural nerve
J M Schröder, G Heide, V Ramaekers, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
January 1, 1984
[Longtime care of spina bifida patients. Therapy and prognosis in the last 20 years]
H H Kramer, W Mortier, R Pothmann, et al.
Page
of 7