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Hammans

Showing results (31-40 of 87) with videos related to

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Case Reports in Gastroenterology|February 17, 2017
Agenesis of the Gallbladder: Role of Clinical Suspicion and Magnetic Resonance to Avoid Unnecessary SurgeryEugenio Tagliaferri, Heinrich Bergmann, Sebastian Hammans, et al.
Geburtshilfe Und Frauenheilkunde|August 1, 1993
[Early amniocentesis between the 12th-14th week of pregnancy. Clinical experiences with 1,100 cases]B Eiben, R Goebel, G Rutt, et al.
COPD|May 26, 2018
Bronchodilator Responses in Respiratory Impedance, Hyperinflation and Gas Trapping in COPDStephen Milne, Christoph Hammans, Stella Watson, et al.
Fetal Diagnosis and Therapy|July 27, 1999
Rapid prenatal diagnosis of aneuploidies in uncultured amniocytes by fluorescence in situ hybridization. Evaluation of >3,000 casesB Eiben, W Trawicki, W Hammans, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 16, 2000
X-linked sideroblastic anaemia with ataxia: another mitochondrial disease?K D Hellier, E Hatchwell, A S Duncombe, et al.
Nature Genetics|May 1, 1993
A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathiesM Brockington, M G Sweeney, S R Hammans, et al.
Journal of Medical Genetics|May 2, 2006
Oculopharyngeal muscular dystrophy: a point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutationD O Robinson, A J Wills, S R Hammans, et al.
Biochemical and Biophysical Research Communications|May 31, 1983
Fluorescence excitation profiles of beta-carotene in solution and in lipid/water mixturesM Van Riel, J Kleinen Hammans, M Van de Ven, et al.
Lancet (London, England)|June 1, 1991
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samplesS R Hammans, M G Sweeney, M Brockington, et al.
Brain : a Journal of Neurology|April 1, 1992
A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathiesS R Hammans, M G Sweeney, D A Wicks, et al.
Pageof 9

Showing results (31-40 of 87) with videos related to

Sort By:
Pageof 9
Case Reports in Gastroenterology|February 17, 2017
Agenesis of the Gallbladder: Role of Clinical Suspicion and Magnetic Resonance to Avoid Unnecessary SurgeryEugenio Tagliaferri, Heinrich Bergmann, Sebastian Hammans, et al.
Geburtshilfe Und Frauenheilkunde|August 1, 1993
[Early amniocentesis between the 12th-14th week of pregnancy. Clinical experiences with 1,100 cases]B Eiben, R Goebel, G Rutt, et al.
COPD|May 26, 2018
Bronchodilator Responses in Respiratory Impedance, Hyperinflation and Gas Trapping in COPDStephen Milne, Christoph Hammans, Stella Watson, et al.
Fetal Diagnosis and Therapy|July 27, 1999
Rapid prenatal diagnosis of aneuploidies in uncultured amniocytes by fluorescence in situ hybridization. Evaluation of >3,000 casesB Eiben, W Trawicki, W Hammans, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 16, 2000
X-linked sideroblastic anaemia with ataxia: another mitochondrial disease?K D Hellier, E Hatchwell, A S Duncombe, et al.
Nature Genetics|May 1, 1993
A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathiesM Brockington, M G Sweeney, S R Hammans, et al.
Journal of Medical Genetics|May 2, 2006
Oculopharyngeal muscular dystrophy: a point mutation which mimics the effect of the PABPN1 gene triplet repeat expansion mutationD O Robinson, A J Wills, S R Hammans, et al.
Biochemical and Biophysical Research Communications|May 31, 1983
Fluorescence excitation profiles of beta-carotene in solution and in lipid/water mixturesM Van Riel, J Kleinen Hammans, M Van de Ven, et al.
Lancet (London, England)|June 1, 1991
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samplesS R Hammans, M G Sweeney, M Brockington, et al.
Brain : a Journal of Neurology|April 1, 1992
A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathiesS R Hammans, M G Sweeney, D A Wicks, et al.
Pageof 9