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1.

Orotic acid: its influence on nuclear RNA and microsomal protein synthesis in brain cells of undernourished rat pups.

Lipp, K; van der Meulen, N; Wenske, G; Linneweh, F.

Biol Neonate ; 33(1-2): 62-5, 1978.

Article in English | MEDLINE | ID: mdl-656522

ABSTRACT

Malnourished rat pups were supplemented with orotic acid. RNA-synthesizing activity of isolated brain cell nuclei and microsomal protein synthesis was measured in vitro. A marked increase was found in the activity of nuclear RNA synthesis but not in microsomal protein synthesis after orotic acid treatment for 7 days.

Subject(s)

Brain/cytology , Cell Nucleus/metabolism , Microsomes/metabolism , Nerve Tissue Proteins/biosynthesis , Nutrition Disorders/drug therapy , Orotic Acid/therapeutic use , RNA/biosynthesis , Animals , Animals, Newborn , Brain/metabolism , Female , Pregnancy , Rats

2.

[Therapy of the nephrotic syndrome in children]. / La terapia della sindrome nefrosica nei bambini.

Linneweh, F.

Minerva Med ; 64(76): 4007-9, 1973 Oct 27.

Article in Italian | MEDLINE | ID: mdl-4764071

Subject(s)

Adrenal Cortex Hormones/therapeutic use , Immunosuppressive Agents/therapeutic use , Nephrosis/drug therapy , Nephrotic Syndrome/drug therapy , Azathioprine/administration & dosage , Child , Child, Preschool , Humans , Nephrosis, Lipoid/drug therapy , Prednisolone/administration & dosage

3.

[Increase of beta-alanine in lymphocytes and thrombocytes for the biochemical diagnosis of cystinosis]. / Beta-Alanin-Vermehrung in Lympho- und Thrombocyten zur biochemischen diagnose der Cystinose.

Wenske, G; Linneweh, F.

Klin Wochenschr ; 50(23): 1082-4, 1972 Dec 01.

Article in German | MEDLINE | ID: mdl-4643485

Subject(s)

Alanine/blood , Blood Platelets/analysis , Cystinosis/blood , Lymphocytes/analysis , Chromatography , Cystine/blood , Cystinosis/genetics , Diseases in Twins , Heterozygote , Humans

4.

[Isotope use in the study of hereditary metabolic diseases]. / Isotopen-Anwendung bei der Erforschung erblicher Stoffwechselkrankheiten.

Linneweh, F.

Monatsschr Kinderheilkd (1902) ; 118(6): 191-4, 1970 Jun.

Article in German | MEDLINE | ID: mdl-4943517

Subject(s)

Deficiency Diseases/enzymology , Glucokinase/metabolism , Infant, Newborn, Diseases/metabolism , Malabsorption Syndromes/metabolism , Metabolism, Inborn Errors/genetics , Phenylketonurias/metabolism , Radioisotopes , Animals , Autoradiography , Blood Glucose/analysis , Brain Chemistry , Carbon Isotopes , Chromatography, Paper , Feces/analysis , Galactose/analysis , Galactose/blood , Galactose/urine , Glucose/analysis , Glycosuria/metabolism , Humans , Infant, Newborn , Leucine , Malabsorption Syndromes/blood , Phenylalanine/analysis , Radioisotope Dilution Technique , Rats , Tritium

5.

[Early biochemical diagnosis of cystinosis from cultured fibroblasts]. / Die biochemische Frühdiagnose der Cystinose aus kultivierten Fibroblasten.

Linneweh, F; Furukawa, T.

Klin Wochenschr ; 48(6): 366-8, 1970 Mar 15.

Article in German | MEDLINE | ID: mdl-5520540

Subject(s)

Cells, Cultured , Cystinosis/diagnosis , Fibroblasts/analysis , Child, Preschool , Culture Techniques , Cystine/analysis , Cystinosis/prevention & control , Cytodiagnosis , Diet Therapy , Humans , Infant , Infant Nutritional Physiological Phenomena , Infant, Newborn , Infant, Newborn, Diseases/diagnosis , Methods , Time Factors

6.

[Galactokinase defect in a newborn infant]. / Galaktokinase-Defekt bei einem Neugeborenen.

Linneweh, F; Schaumlöffel, E; Vetrella, M.

Klin Wochenschr ; 48(1): 31-3, 1970 Jan 01.

Article in German | MEDLINE | ID: mdl-5522111

Subject(s)

Erythrocytes/enzymology , Glucokinase/analysis , Infant, Newborn, Diseases/enzymology , Metabolism, Inborn Errors/diagnosis , Carbon Isotopes , Cataract/genetics , Chromatography, Paper , Chromatography, Thin Layer , Diet Therapy , Ethnicity , Female , Galactose/blood , Galactose/metabolism , Galactose/urine , Humans , Infant, Newborn , Infant, Newborn, Diseases/diagnosis , Infant, Newborn, Diseases/therapy , Metabolism, Inborn Errors/enzymology , Metabolism, Inborn Errors/therapy , Oxidation-Reduction , RNA Nucleotidyltransferases/analysis

7.

[Experience with automatic amino acid analysis in ultra micro range]. / Uber Erfahrungen mit der vollautomatischen Aminosäuren-Analyse im Ultra-Mikrobereich.

Linneweh, F; Barthelmai, W; Wenske, G.

Klin Wochenschr ; 47(18): 971-5, 1969 Sep 15.

Article in German | MEDLINE | ID: mdl-5376914

Subject(s)

Amino Acids/analysis , Autoanalysis , Amino Acids/blood , Animals , Autoanalysis/instrumentation , Blood Platelets/analysis , Chromatography , Conjunctiva/analysis , Humans , Insecta , Leukocytes/analysis

8.

[Therapy of the nephrotic syndrome in childhood]. / Therapie des nephrotischen Syndroms im Kindesalter.

Linneweh, F.

Dtsch Med Wochenschr ; 94(25): 1335-6, 1969 Jun 20.

Article in German | MEDLINE | ID: mdl-5785299

Subject(s)

Azathioprine/therapeutic use , Nephrotic Syndrome/drug therapy , Prednisolone/therapeutic use , Azathioprine/adverse effects , Biopsy , Blood Proteins/analysis , Humans , Kidney/pathology

9.

[Clinical aspects of acute diffuse glomerulonephritis]. / Die Klinik der akuten diffusen Glomerulonephritis.

Linneweh, F.

Monatsschr Kinderheilkd (1902) ; 117(4): 296-303, 1969 Apr.

Article in German | MEDLINE | ID: mdl-5377538

Subject(s)

Glomerulonephritis , Acute Disease , Adolescent , Anti-Glomerular Basement Membrane Disease/diagnosis , Arteritis/diagnosis , Cardiac Output , Child , Child, Preschool , Collagen Diseases/diagnosis , Diagnosis, Differential , Glomerulonephritis/complications , Glomerulonephritis/diagnosis , Glomerulonephritis/drug therapy , Glomerulonephritis/etiology , Glomerulonephritis/therapy , Humans , Hypertension, Renal/etiology , Nephritis/diagnosis , Penicillins/therapeutic use , Prognosis , Purpura/diagnosis , Reserpine/therapeutic use , Streptococcal Infections , Tonsillectomy , Water-Electrolyte Balance

10.

[Malabsorption in hereditary disorders of the carbohydrate and amino acid metabolism]. / Malabsorption bei hereditären Störungen des Kohlenhydrat- und Aminosäuren-Stoffwechsels.

Linneweh, F.

Acta Paediatr Acad Sci Hung ; 10(1): 1-12, 1969.

Article in German | MEDLINE | ID: mdl-5793288

Subject(s)

Amino Acid Metabolism, Inborn Errors/complications , Carbohydrate Metabolism, Inborn Errors/complications , Malabsorption Syndromes/etiology , Animals , Cystinuria , Galactose/metabolism , Glucose/metabolism , Hartnup Disease , Humans , Phenylketonurias , Rats

11.

[Carbohydrate composition of plant nutrients as the basis for the diet therapy of hereditary metabolic disorders]. / Die Kohlenhydrat-Zusammensetzung pflanzlicher Nahrungsmittel als Grundlage der dlätetischen Behandlung erblicher Stoffwechselstörungen.

Göthe, S; Linneweh, F.

Klin Wochenschr ; 46(9): 468-74, 1968 May 01.

Article in German | MEDLINE | ID: mdl-5674109

Subject(s)

Carbohydrate Metabolism, Inborn Errors/therapy , Carbohydrates/analysis , Plants, Edible/analysis , Chromatography, Paper , Diet Therapy , Food Analysis , Fruit/analysis , Galactose/metabolism , Galactosemias/therapy , Humans , Lactose Intolerance/therapy , Malabsorption Syndromes/therapy , Sucrose/metabolism , Vegetables/analysis

12.

[Absorption studies in hereditary mono- and disaccharide malabsorptions]. / Resorptionsstudien bei hereditären Mono- und Disaccharidmalabsorptionen.

Schaumlöffel, E; Linneweh, F; Graul, E H.

Nucl Med (Stuttg) ; : 23-8, 1967.

Article in German | MEDLINE | ID: mdl-5601744

Subject(s)

Disaccharides/metabolism , Intestinal Absorption , Malabsorption Syndromes/genetics , Monosaccharides/metabolism , Carbon Isotopes , Child , Female , Fructose/metabolism , Galactose/metabolism , Glucose/metabolism , Glucose Tolerance Test , Humans , Infant , Malabsorption Syndromes/enzymology , Malabsorption Syndromes/etiology , Maltose/metabolism

13.

[On the residual activity of defective enzymes in hereditary monosaccharide and disaccharide malabsorption]. / Uber die Restaktivität defekter Enzyme bei hereditärer Mono- und Disaccharid- Malabsorption.

Linneweh, F; Schaumlöffel, E; Graul, E H; Bode, H H.

Schweiz Med Wochenschr ; 96(13): 424-7, 1966 Apr 02.

Article in German | MEDLINE | ID: mdl-5984005

Subject(s)

Galactose/metabolism , Glucose/metabolism , Malabsorption Syndromes/genetics , Maltose/metabolism , Sucrose/metabolism , Carbon Isotopes , Child , Glucose Tolerance Test , Humans , Infant , Molecular Biology

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