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Biomedical subjects

B Ludwig

Publications and source records attributed to B Ludwig.

180 records · Page 10Linked to original sources

Cerebral seizures of probable orbitofrontal origin.

Four patients with seizures of presumed temporal lobe origin are presented in whom a definite focal ictal onset in the orbitofrontal cortex was revealed during recording, either by chronically implanted electrodes or ECoG. In three cases automatisms occurred concomitantly with orbitofrontal activation without spread of paroxysmal activity into the temporal structures monitored. With eight additional cases of possible orbitofrontal epilepsy found on reviewing the literature, two subgroups emerge: (1) patients with primarily psychomotor-type fits, and (2) patients with loss of consciousness, head and eye deviation, and generalized convulsions. Scalp EEGs, in patients on whom we have available data, manifested bilaterally synchronous, paroxysmal discharges which were bifrontal, frontopolar, or maximal in one anterior quadrant, with or without evidence of additional temporal lobe involvement. On the basis of anatomic and physiological studies, as well as our own electrographic data, it is felt that a posterior orbitofrontal and temporo-limbic relationship exists, within which autonomous epileptogenic zones may develop, with the ability to discharge directly and independently to subcortical centers, while eliciting similar clinical patterns.

Adolescent↗

Characterization of the CuA center in the cytochrome c oxidase from Thermus thermophilus for the spectral range 1800-500 cm-1 with a combined electrochemical and Fourier transform infrared spectroscopic setup.

In this study we present the electrochemically induced Fourier transform infrared (FTIR) difference spectra of the Cu(A) center derived from the ba(3)-type cytochrome c oxidase of Thermus thermophilus in the spectral range from 1800 to 500 cm(-1). The mid infrared is dominated by the nu(C[double bond]O) vibrations of the amide I modes at 1688, 1660, and 1635 cm(-1), reflecting the redox-induced perturbation of the predominantly beta-sheet type structure. The corresponding amide II signal is found at 1528 cm(-1). In the lower frequency range below 800 cm(-1), modes from amino acids liganding the Cu(A) center are expected. On the basis of the absorbance spectrum of the isolated amino acids, methionine is identified as an important residue, displaying C-S vibrations at these frequencies. This spectral range was previously disregarded by protein IR spectroscopists, mainly due to the strong absorbance of the solvent, H(2)O. With an optimized setup, however, IR is found suitable for structure/function studies on proteins.

Amino Acids↗

Cloning of Paracoccus cytochrome c oxidase subunit II.

Cytochrome c oxidase from Paracoccus denitrificans is composed of two subunits, yet is active in both electron transport and proton translocation. A cloning approach and immunologic screening protocol is described for the isolation of the subunit II gene expressed in E. coli. DNA sequencing should establish the extent of homology to eukaryotic oxidase.

Cloning, Molecular↗

[Intraspinal anomalies in myelomeningocele].

This study reports the results of MRI analysis of the spinal cord in 83 patients with myelomeningocele. 63 patients had a "tethered cord" or a "suspected tethered cord". In 14 cases we found a "hydro-/syringomyelia". In only 2 cases there were no pathological findings. The influence especially of the "tethered cord" and the "hydro-/syringomyelia" on the development of deformities of the locomotor apparatus is discussed. Concerning this problem the experience reported in the literature is not sufficient enough to make final statements. However, in cases of deterioration of the neurological status in patients with myelomeningocele the influence of intraspinal anomalies should be considered giving rise to further diagnostic examinations.

Adolescent↗

[Rathbun syndrome (hypophosphatasia). Clinical aspects: dwarfism and Bechterew symptoms].

We report on a 43-year-old patient with short stature (hyposomia), allegedly the result of vitamin-D-resistant rickets, previously treated for ankylosing spondylitis. In addition, a uricostatic drug therapy was also necessary because of hyperuricemia with gout attacks. Further examinations revealed the accurate diagnosis: Rathbun's disease. Hypophosphatasia is a hereditary disorder characterized by a deficiency of liver/bone/kidney alkaline phosphatase activity in serum and tissues with defective bone mineralization, bone deformities, short stature, early loss of teeth, and craniosynostosis. In our patient radiographic features were spinal hyperostosis, but with syndesmophytes, chondrocalcinosis of peripheral joints and intervertebral discs, calcific periarthritis and premature closure of skull sutures. Curved ribs and short stature were suggestive of rickets. The aim of this case report is to demonstrate the close relations between hypophosphatasia and spondylitis ankylosans in respect to radiology and clinical symptoms.

Adult↗

Dyke Postmortem CT and Award. autopsy in perinatal intracranial hemorrhage.

To improve interpretation of intracranial computed tomographic findings in vivo, postmortem computed tomography was correlated directly with autopsy findings in 105 specimens of human stillborn and live-birth infants, ranging in age from gestational week 13 to postnatal month 18. This study identifies the typical computed tomographic appearance of intradural and other hemorrhages, attempts to correlate the type of hemorrhage with brain maturity, and documents that postmortem computed tomography is useful to the neuropathologist as a supplementary method complementing the traditional postmortem examination.

Brain↗

Cranial computed tomography in disorders of complex carbohydrate metabolism and related storage diseases.

Computed tomography (CT) was performed on 34 children with different disorders of complex carbohydrate metabolism and related storage diseases to obtain data on the degree of cerebral involvement. The main findings on CT were cerebral atrophy and hypodensity of the white matter. There was a great variability in these CT findings, even in siblings. Among the patients there were several in whom CT was normal, so a negative study does not exclude one of these disorders. These findings show that CT features such as cerebral atrophy or hypodensity are helpful in the evaluation of these disorders, though a diagnosis cannot be made on the basis of CT alone.

Brain Diseases, Metabolic↗