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Archives of Disease in Childhood
|
September 1, 1994
De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1)
P E Jardine, M C Koch, P W Lunt, et al.
Schweizer Archiv Fur Tierheilkunde
|
October 12, 2023
Virus discovery in dogs with non-suppurative encephalitis reveals a high incidence of tick-borne encephalitis virus infections in Switzerland
K L D Dawson, N Wildi, M C Koch, et al.
Archives of Neurology
|
January 1, 1995
Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy
K Ricker, M C Koch, F Lehmann-Horn, et al.
Clinical Rheumatology
|
September 1, 1986
The arthritis of hemochromatosis. A review of 25 cases with special reference to chondrocalcinosis, and a comparison with patients with primary hyperparathyroidism and controls
J P Huaux, A Geubel, M C Koch, et al.
Neuromuscular Disorders : NMD
|
September 21, 2000
Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2)
W Kress, B Mueller-Myhsok, K Ricker, et al.
Human Molecular Genetics
|
May 1, 1995
Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)
P W Lunt, P E Jardine, M C Koch, et al.
Geburtshilfe Und Frauenheilkunde
|
August 8, 2014
Introduction of Inhaled Nitrous Oxide and Oxygen for Pain Management during Labour - Evaluation of Patients' and Midwives' Satisfaction
U Dammer, C Weiss, E Raabe, et al.
Neurology
|
January 1, 1997
Proximal myotonic myopathy with MRI white matter abnormalities of the brain
E Hund, O Jansen, M C Koch, et al.
Teratology
|
April 26, 2001
A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects
K Stegmann, J Boecker, B Richter, et al.
Science (New York, N.Y.)
|
August 7, 1992
The skeletal muscle chloride channel in dominant and recessive human myotonia
M C Koch, K Steinmeyer, C Lorenz, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 59) with videos related to
Sort By:
Page
of 6
Archives of Disease in Childhood
|
September 1, 1994
De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1)
P E Jardine, M C Koch, P W Lunt, et al.
Schweizer Archiv Fur Tierheilkunde
|
October 12, 2023
Virus discovery in dogs with non-suppurative encephalitis reveals a high incidence of tick-borne encephalitis virus infections in Switzerland
K L D Dawson, N Wildi, M C Koch, et al.
Archives of Neurology
|
January 1, 1995
Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy
K Ricker, M C Koch, F Lehmann-Horn, et al.
Clinical Rheumatology
|
September 1, 1986
The arthritis of hemochromatosis. A review of 25 cases with special reference to chondrocalcinosis, and a comparison with patients with primary hyperparathyroidism and controls
J P Huaux, A Geubel, M C Koch, et al.
Neuromuscular Disorders : NMD
|
September 21, 2000
Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2)
W Kress, B Mueller-Myhsok, K Ricker, et al.
Human Molecular Genetics
|
May 1, 1995
Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)
P W Lunt, P E Jardine, M C Koch, et al.
Geburtshilfe Und Frauenheilkunde
|
August 8, 2014
Introduction of Inhaled Nitrous Oxide and Oxygen for Pain Management during Labour - Evaluation of Patients' and Midwives' Satisfaction
U Dammer, C Weiss, E Raabe, et al.
Neurology
|
January 1, 1997
Proximal myotonic myopathy with MRI white matter abnormalities of the brain
E Hund, O Jansen, M C Koch, et al.
Teratology
|
April 26, 2001
A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects
K Stegmann, J Boecker, B Richter, et al.
Science (New York, N.Y.)
|
August 7, 1992
The skeletal muscle chloride channel in dominant and recessive human myotonia
M C Koch, K Steinmeyer, C Lorenz, et al.
Page
of 6