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Your search keyword '"Wehinger H"' showing total 34 results
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34 results on '"Wehinger H"'

9. Heterozygoter NADH-Meth�moglobin-Reduktase-Defekt mit Meth�moglobin�mie bei einem S�gling

Author

Wehinger H, Schuchmann L, Wilhelm Künzer, Seibert G, Gunkel J, and Irene Witt

Subjects
Gynecology, medicine.medical_specialty, business.industry, Pediatrics, Perinatology and Child Health, medicine, NADH methemoglobin reductase, Methemoglobinemia, medicine.disease, business
Abstract

Bei einem weiblichen Saugling kam es im Alter von 3 Wochen im Verlaufe einer Dyspepsie akut zu einer erheblichen Methamoglobinamie von 18% des vorhandenen Hamoglobins. In den folgenden Monaten traten wiederholt dyspeptische Schube auf, die jeweils mit einem Anstieg der Methamoglobin-Konzentration, zeitweise bis 50%, verbunden waren. In den Erythrocyten des Kindes wurde eine auf 50% des Normalwertes verminderte Aktivitat der NADH-abhangigen Methamoglobin-Reduktase gefunden. Offensichtlich handelt es sich um einen heterozygoten Enzymdefekt. Bei der Untersuchung der Familie wurden 13 weitere heterozygote Defekttrager beobachtet. Das Auftreten einer schweren Methamoglobinamie ist bei heterozygotem Reduktasemangel sehr selten. Bei unserer Patientin hat vermutlich eine wahrend der Dyspepsien entstandene Noxe zur vermehrten Bildung von Methamoglobin gefuhrt. Da Neugeborene nur 50% der Methamoglobin-Reduktase-Aktivitat von Erwachsenen haben, kommt es bei einem gleichzeitigen Methamoglobin-Reduktase-Defekt nicht zu einer ausreichenden Reduktion des entstandenen Methamoglobins.

Published
1973

10. [Vitamin D deficiency rickets after vitamin D hypersensitivity with subcutaneous fat necrosis in the newborn period]

Author

Wehinger H

Subjects
medicine.medical_specialty, Necrosis, Hypercalcaemia, Period (gene), chemistry.chemical_element, Rickets, Calcium, vitamin D deficiency, Infant, Newborn, Diseases, Diagnosis, Differential, Drug Hypersensitivity, Internal medicine, medicine, Vitamin D and neurology, Humans, Vitamin D, Asphyxia Neonatorum, business.industry, Infant, Newborn, Calcinosis, Infant, medicine.disease, Radiography, Endocrinology, chemistry, Adipose Tissue, Pediatrics, Perinatology and Child Health, Toxicity, Hypercalcemia, medicine.symptom, business
Published
1969

15. Densitometrisch-quantitative Bestimmung von Hämoglobin A2 nach Mikrozonen-Elektrophorese auf Cellulose-Acetat-Folie

Author

Wehinger, H. and Alebouyeh, M.

Abstract

Zusammenfassung Eine einfache Methode zur schnellen quantitativen Bestimmung von Hämoglobin A2 wird mitgeteilt. Dabei werden die Hämoglobine im Beckman-Spinco Mikrozonenelektrophorese-System auf Cellulose-Acetat-Folie unter Verwendung eines diskontinuierlichen Puffersystems getrennt. Nach Färbung mit Ponceau S werden die Pherogramme densitometrisch ausgewertet. Die Methode genügt den Anforderungen der Diagnostik heterozygoterß-Thalassämie-Träger.

Published
1970
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16. [Therapy of the hemolytic-uremic syndrome].

Author

Wehinger H, Sutor HA, Schindera F, and Künzer W

Subjects
Aspirin therapeutic use, Dipyridamole therapeutic use, Hemolytic-Uremic Syndrome drug therapy, Heparin therapeutic use, Humans, Methods, Peritoneal Dialysis, Platelet Adhesiveness drug effects, Streptokinase therapeutic use, Hemolytic-Uremic Syndrome therapy
Published
1974
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17. [Dimensions of pathology in pediatrics--based on hematologic examples].

Author

Wehinger H

Subjects
Adolescent, Age Factors, Anemia, Hypochromic diagnosis, Child, Child, Preschool, Diagnosis, Differential, Erythroblastosis, Fetal diagnosis, Female, Humans, Infant, Infant, Newborn, Male, Pregnancy, Thalassemia diagnosis, Hematologic Diseases diagnosis, Hematologic Diseases epidemiology, Hematologic Diseases etiology
Published
1974

18. Prophylactic central nervous system therapy with cranial irradiation and intrathecal methotrexate in acute lymphoblastic leukemia of childhood.

Author

Wehinger H, Slanina J, Jacobi H, Musshoff K, Dietz V, Sauer M, and Dilger M

Subjects
Adolescent, Asparaginase therapeutic use, Child, Child, Preschool, Cobalt Radioisotopes therapeutic use, Drug Therapy, Combination, Electroencephalography, Humans, Infant, Injections, Spinal, Leukemia, Lymphoid drug therapy, Leukemia, Lymphoid radiotherapy, Methotrexate adverse effects, Prednisone therapeutic use, Radioisotope Teletherapy, Radiotherapy adverse effects, Radiotherapy Dosage, Vincristine therapeutic use, Leukemia, Lymphoid therapy, Meningism prevention & control, Methotrexate therapeutic use
Published
1974

20. [Symptoms and therapy for acute and subacute digitalis poisoning in newborn and older infants].

Author

Windorfer A Jr, Wehinger H, and Schumacher G

Subjects
Acute Disease, Biological Transport, Active, Digoxin therapeutic use, Female, Humans, Infant, Newborn, Infant, Newborn, Diseases drug therapy, Infant, Premature, Infant, Premature, Diseases diagnosis, Magnesium therapeutic use, Male, Phenytoin therapeutic use, Poisoning diagnosis, Poisoning drug therapy, Potassium therapeutic use, Respiratory Distress Syndrome, Newborn drug therapy, Sodium, Vomiting chemically induced, Digoxin poisoning, Infant, Newborn, Diseases diagnosis
Published
1973

21. [NBT-test, a new aid in the diagnosis of bacterial infections].

Author

Kim SK, Monz E, and Wehinger H

Subjects
Age Factors, Collagen Diseases diagnosis, Diagnosis, Differential, Fever diagnosis, Hemophilia A diagnosis, Humans, Infant, Newborn, Methods, Tetrazolium Salts, Tuberculosis diagnosis, Virus Diseases diagnosis, Bacterial Infections diagnosis
Published
1973

22. [On the clinical picture and pathological anatomy of the maple syrup disease ("branded chain ketoaciduria"). Report on 2 cases in 1 family].

Author

Sander C, Clotten R, Noetzel H, and Wehinger H

Subjects
Body Height, Body Weight, Diet Therapy, Humans, Infant, Infant, Newborn, Isoleucine blood, Keto Acids urine, Leucine blood, Male, Maple Syrup Urine Disease pathology, Maple Syrup Urine Disease therapy, Prognosis, Valine blood, Infant, Newborn, Diseases genetics, Maple Syrup Urine Disease genetics
Published
1968
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23. [Diagnostic and therapeutic problems in Ivemark's syndrome (Asplenia-Syndrome)].

Author

Schumacher G, Schenck W, Schlosser V, Wehinger H, Gunkel J, and Schuchmann L

Subjects
Abnormalities, Multiple diagnosis, Abnormalities, Multiple mortality, Angiocardiography, Blood Coagulation Tests, Blood Platelets, Cineangiography, Disseminated Intravascular Coagulation etiology, Female, Heart Defects, Congenital diagnosis, Heparin therapeutic use, Humans, Infant, Infant, Newborn, Karyotyping, Male, Postoperative Complications, Situs Inversus diagnostic imaging, Syndrome, Heart Defects, Congenital surgery, Situs Inversus surgery, Spleen abnormalities
Published
1972

24. [Familial deficiency on alpha-1-antitrypsin].

Author

Wehinger H, Karitzky D, and Witt I

Subjects
Adult, Blood Coagulation Tests, Blood Donors, Blood Protein Electrophoresis, Child, Female, Heterozygote, Homozygote, Humans, Immunoelectrophoresis, Infant, Male, Metabolism, Inborn Errors blood, Middle Aged, Pedigree, Metabolism, Inborn Errors genetics, Trypsin Inhibitors blood
Published
1971

26. [Heterozygous NADH-methemoglobin reductase defect with methemoglobinemia in an infant (author's transl)].

Author

Witt I, Gunkel J, Seibert G, Wehinger H, Schuchmann L, and Künzer W

Subjects
Diarrhea, Infantile complications, Erythrocytes enzymology, Female, Fetal Hemoglobin analysis, Humans, Infant, Newborn, Metabolism, Inborn Errors complications, Metabolism, Inborn Errors enzymology, Methemoglobin analysis, Methemoglobinemia complications, Methemoglobinemia etiology, Pedigree, Heterozygote, Metabolism, Inborn Errors genetics, Methemoglobinemia enzymology, NADH, NADPH Oxidoreductases blood
Published
1973

27. [Erythrocyte carbonic anhydrases in various diseases of childhood].

Author

Wehinger H

Subjects
Adolescent, Age Factors, Anemia, Hypochromic enzymology, Carbonic Anhydrases biosynthesis, Child, Child, Preschool, Down Syndrome enzymology, Heart Defects, Congenital enzymology, Humans, Infant, Leukemia, Myeloid enzymology, Respiratory Insufficiency enzymology, Thalassemia enzymology, Thyroid Hormones pharmacology, Carbonic Anhydrases blood, Erythrocytes enzymology
Published
1973

33. [Studies with a modified cytochemical NBT test].

Author

Wehinger H and Kim SK

Subjects
Bacterial Infections diagnosis, Birth Weight, Candidiasis diagnosis, Child, Collagen Diseases diagnosis, Endotoxins pharmacology, Gestational Age, Hemophilia A diagnosis, Humans, Infant, Newborn, Infant, Premature, Meningococcal Infections diagnosis, Sepsis diagnosis, Steroids pharmacology, Tetrazolium Salts, Time Factors, Tuberculosis diagnosis, Virus Diseases diagnosis, Phagocyte Bactericidal Dysfunction diagnosis
Published
1973

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