BIOMAT Database Logo BIOMAT Database Logo

[Prenatal diagnosis of glycogenosis type II (Pompe) and subsequent therapeutic abortion (author's transl)]. 1974

J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007226 Infant Mortality Postnatal deaths from BIRTH to 365 days after birth in a given population. Postneonatal mortality represents deaths between 28 days and 365 days after birth (as defined by National Center for Health Statistics). Neonatal mortality represents deaths from birth to 27 days after birth. Neonatal Mortality,Mortality, Infant,Postneonatal Mortality,Infant Mortalities,Mortalities, Infant,Mortalities, Neonatal,Mortalities, Postneonatal,Mortality, Neonatal,Mortality, Postneonatal,Neonatal Mortalities,Postneonatal Mortalities
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D008247 Lysosomes A class of morphologically heterogeneous cytoplasmic particles in animal and plant tissues characterized by their content of hydrolytic enzymes and the structure-linked latency of these enzymes. The intracellular functions of lysosomes depend on their lytic potential. The single unit membrane of the lysosome acts as a barrier between the enzymes enclosed in the lysosome and the external substrate. The activity of the enzymes contained in lysosomes is limited or nil unless the vesicle in which they are enclosed is ruptured or undergoes MEMBRANE FUSION. (From Rieger et al., Glossary of Genetics: Classical and Molecular, 5th ed). Autolysosome,Autolysosomes,Lysosome
D008297 Male Males
D008854 Microscopy, Electron Microscopy using an electron beam, instead of light, to visualize the sample, thereby allowing much greater magnification. The interactions of ELECTRONS with specimens are used to provide information about the fine structure of that specimen. In TRANSMISSION ELECTRON MICROSCOPY the reactions of the electrons that are transmitted through the specimen are imaged. In SCANNING ELECTRON MICROSCOPY an electron beam falls at a non-normal angle on the specimen and the image is derived from the reactions occurring above the plane of the specimen. Electron Microscopy
D009129 Muscle Tonus The state of activity or tension of a muscle beyond that related to its physical properties, that is, its active resistance to stretch. In skeletal muscle, tonus is dependent upon efferent innervation. (Stedman, 25th ed) Muscle Tension,Muscle Tightness,Muscular Tension,Tension, Muscle,Tension, Muscular,Tightness, Muscle,Tonus, Muscle
D009132 Muscles Contractile tissue that produces movement in animals. Muscle Tissue,Muscle,Muscle Tissues,Tissue, Muscle,Tissues, Muscle
D009202 Cardiomyopathies A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS). Myocardial Disease,Myocardial Diseases,Myocardial Diseases, Primary,Myocardial Diseases, Secondary,Myocardiopathies,Primary Myocardial Disease,Cardiomyopathies, Primary,Cardiomyopathies, Secondary,Primary Myocardial Diseases,Secondary Myocardial Diseases,Cardiomyopathy,Cardiomyopathy, Primary,Cardiomyopathy, Secondary,Disease, Myocardial,Disease, Primary Myocardial,Disease, Secondary Myocardial,Diseases, Myocardial,Diseases, Primary Myocardial,Diseases, Secondary Myocardial,Myocardial Disease, Primary,Myocardial Disease, Secondary,Myocardiopathy,Primary Cardiomyopathies,Primary Cardiomyopathy,Secondary Cardiomyopathies,Secondary Cardiomyopathy,Secondary Myocardial Disease
D011247 Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. Gestation,Pregnancies

Related Publications

J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer
Prenatal diagnosis of type-II glycogenosis.
May 1970, Lancet (London, England),
J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer
[Biochemical diagnosis of glycogenosis type II (acid maltase deficiency) (author's transl)].
December 1977, Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie,
J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer
[Differential diagnosis in anorexia nervosa: glycogenosis II (the Pompe type)].
August 1999, Deutsche medizinische Wochenschrift (1946),
J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer
Muscular form of glycogenosis, type II (Pompe).
June 1967, Neurology,
J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer
Enzyme therapy and prenatal diagnosis in glycogenosis type II.
November 1974, American journal of diseases of children (1960),
J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer
[Atypical clinical forms of Type II glycogenosis (Pompe)].
January 1982, Verhandlungen der Deutschen Gesellschaft fur Pathologie,
J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer
[The physiological segregation of glycogen. A precondition of the liver cell changes in glycogenosis type II (Pompe) (author's transl)].
January 1971, Verhandlungen der Deutschen Gesellschaft fur Pathologie,
J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer
Acid alpha-glucosidase deficiency (glycogenosis type II, Pompe disease).
March 2002, Current molecular medicine,
J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer
[Glycogenosis type I. Therapy (author's transl)].
August 1980, Anales espanoles de pediatria,
J Schaub, and M Osang, and D B von Bassewitz, and W Grote, and R Terinde, and I Lombeck, and H J Bremer
Approach to gene therapy of glycogenosis type II (Pompe disease).
July 2000, Molecular genetics and metabolism,
Copied contents to your clipboard!