Page last updated: 2024-08-23

transferrin and Syndrome

transferrin has been researched along with Syndrome in 48 studies

Research

Studies (48)

Timeframe	Studies, this research(%)	All Research%
pre-1990	13 (27.08)	18.7374
1990's	24 (50.00)	18.2507
2000's	7 (14.58)	29.6817
2010's	3 (6.25)	24.3611
2020's	1 (2.08)	2.80

Authors

Authors	Studies
Bramania, PK; Bramania, R; Furia, FF; Mahmoud, M; Ruggajo, P	1
Bastaki, F; Hamici, S; Khalifa, M	1
Al-Gazali, L; Al-Jasmi, F; Antonarakis, SE; Arnold, SJ; Bakey, Z; El-Shanti, H; Eng, CM; Hamamy, H; He, W; Helmstädter, M; Hertecant, J; Hunter, JV; Kambouris, M; Karami Madani, G; Karimiani, EG; Liu, P; Lunke, S; Makrythanasis, P; Maroofian, R; Najafi, M; Petersen, A; Rad, A; Rajab, A; Rehman, AU; Richmond, C; Santoni, FA; Schmidts, M; Stark, Z; Tokita, MJ; Vetrini, F; Walkiewicz, M; Wu, K; Xia, F; Yang, Y	1
Breeding, L; Darvin, K; Espinoza, SE; Halade, D; Ovalles, S; Randolph, A; Richardson, A	1
Chiang, CK; Ho, LC; Hu, FC; Huang, JW; Hung, KY; Peng, YS; Wang, HH; Wu, KD	1
Bubel, S; Hackler, R; Hagenah, J; Hoffmann, GF; Klein, C; Peters, V; Schaefer, JR; Vieregge, P	1
Garderet, L; Gorin, NC; Hermelin, B; Rosmorduc, O	1
Coucke, P; Gillessen-Kaesbach, G; Grünewald, S; Morava, E; Smeitink, J; Voit, T; Wevers, R; Wopereis, S	1
O'Brien, JF	1
De Meirleir, L; Huijben, K; Keymolen, K; Korsch, E; Lefeber, DJ; Matthijs, G; Morava, E; Wevers, RA; Wopereis, S; Zeevaert, R	1
Beck, MM; Kuenzel, WJ	1
Bozhko, GKh; Kostiukovskaia, LS; Kryzhenko, TV; Kulabukhov, VM; Voloshin, PV	1
Barrière, H; Mussini, JM; Planchon, B	1
Lange, V	1
Skovby, F; Stibler, H	1
Gray, RG; Hutchesson, AC; Keir, G; Spencer, DA	1
Clayton, P; Dell, A; di-Tomaso, E; Keir, G; Mian, N; Reason, A; Winchester, B	1
Clayton, PT; Mian, N	1
Hanefeld, F; Knauer, R; Lehle, L; von Figura, K	1
Yamashita, K	1
Buist, N; Diaz, S; Freeze, H; Manzi, A; Paneerselvam, K; Powell, LD; Varki, A; Vij, R	1
Gavalov, SM; Soboleva, MK	1
Gu, J; Inui, K; Okamoto, N; Wada, Y	1
Ideo, H; Kanai, M; Ohkura, T; Ohno, K; Yamashita, K	1
Carchon, H; Jaeken, J; Stibler, H	1
Brostrøm, K; Petersen, MB; Skovby, F; Stibler, H	1
Fukushima, K; Ideo, H; Ohkura, T; Ohno, K; Takeshita, K; Yamashita, K; Yuasa, I	1
Cederberg, B; Stibler, H	1
Pedersen, SJ; Strøm, EH; Strømme, P; Westvik, J	1
Brissot, P; Deugnier, Y; Loréal, O; Moirand, R; Mortaji, AM; Paillard, F	1
Alton, G; Freeze, HH; Harms, E; Harms, HK; Hasilik, M; Koch, HG; Körner, C; Marquardt, T; Niehues, R; Reiter, K; Schiebe-Sukumar, M; von Figura, K; Wu, R; Zimmer, KP	1
Ferrannini, E	1
Fehér, J; Jakab, L; Pozsonyi, T	1
Gekova, K; Georgieva, B; Gigova, D	1
Inui, K; Nishikawa, A; Okada, S; Okamoto, N; Taniguchi, N; Tsukamoto, H; Wada, Y	1
Akaboshi, S; Ehara, H; Itoh, M; Ochiai, Y; Ohno, K; Takeshita, K; Yoshida, K; Yuasa, I	1
Harbison, MD; Harrison, HH; Miller, KL; Slonim, AE	1
Hagberg, B; Kristiansson, B; Strömland, K	1
Clayton, PT; Hall, NA; Harding, BN; Horslen, SP; Keir, G; Winchester, B	1
Maehlen, J; Strøm, EH; Strømme, P; Torvik, A	1
Jaeken, J; Stibler, H	1
Andersson, M; Hagberg, B; Kristiansson, B; Tonnby, B	1
Jaeken, J	1
Killian, W; Linkesch, W; Riederer, P	1
Bias, WB; Lichtenstein, J; Rivas, ML	1
Havlik, E; Höfer, R; Pietschmann, VH; Willvonseder, R	1
Bokisch, VA; Dixon, FJ; Müller-Eberhard, HJ; Russell, PK; Top, FH	1
al-Rashid, RA	1

Reviews

5 review(s) available for transferrin and Syndrome

Article	Year
Exome sequence identified a c.320A > G ALG13 variant in a female with infantile epileptic encephalopathy with normal glycosylation and random X inactivation: Review of the literature. European journal of medical genetics, 2017, Volume: 60, Issue:10 Topics: Child, Preschool; Congenital Disorders of Glycosylation; Exome; Female; Glycosylation; Heterozygote; Humans; Infant; Mental Retardation, X-Linked; Mutation, Missense; N-Acetylglucosaminyltransferases; Protein Processing, Post-Translational; Spasms, Infantile; Syndrome; Transferrin; X Chromosome Inactivation	2017
Methods for detection of carbohydrate-deficient glycoprotein syndromes. Seminars in pediatric neurology, 2005, Volume: 12, Issue:3 Topics: Carbohydrates; Glycoproteins; Glycosylation; Humans; Mass Spectrometry; Metabolic Diseases; Syndrome; Transferrin	2005
The carbohydrate-deficient glycoprotein syndrome: an experiment of nature in glycosylation. Biochemical Society transactions, 1995, Volume: 23, Issue:1 Topics: Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Glycoproteins; Glycosylation; Humans; Syndrome; Transferrin	1995
[Carbohydrate-deficient glycoprotein syndrome: N-linked oligosaccharide transfer deficiency]. Seikagaku. The Journal of Japanese Biochemical Society, 1994, Volume: 66, Issue:11 Topics: Carbohydrate Metabolism, Inborn Errors; Endoplasmic Reticulum; Female; Glycoproteins; Humans; Male; Syndrome; Transferrin	1994
The carbohydrate-deficient glycoprotein syndromes: pre-Golgi and Golgi disorders? Glycobiology, 1993, Volume: 3, Issue:5 Topics: Carbohydrate Metabolism, Inborn Errors; Carbohydrate Sequence; Female; Glycoproteins; Humans; Male; Molecular Sequence Data; Syndrome; Transferrin	1993

Other Studies

43 other study(ies) available for transferrin and Syndrome

Article	Year
Prevalence of malnutrition inflammation complex syndrome among patients on maintenance haemodialysis at Muhimbili National Hospital in Tanzania: a cross-sectional study. BMC nephrology, 2020, 11-30, Volume: 21, Issue:1 Topics: Adolescent; Adult; Aged; C-Reactive Protein; Cholesterol; Creatinine; Cross-Sectional Studies; Female; Ferritins; Hemoglobins; Humans; Inflammation; Kidney Failure, Chronic; Male; Malnutrition; Middle Aged; Prevalence; Prospective Studies; Renal Dialysis; Serum Albumin; Syndrome; Tanzania; Thinness; Transferrin; Young Adult	2020
Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function. Human mutation, 2019, Volume: 40, Issue:3 Topics: Adult; Alleles; Child; Child, Preschool; Endocytosis; Endosomes; Female; Fibroblasts; Homozygote; Humans; Infant; Infant, Newborn; Loss of Function Mutation; Male; Myelin Sheath; Neurodevelopmental Disorders; Pedigree; Phosphoprotein Phosphatases; Syndrome; Transferrin	2019
Plasma protein biomarkers of the geriatric syndrome of frailty. The journals of gerontology. Series A, Biological sciences and medical sciences, 2014, Volume: 69, Issue:2 Topics: Aged; Aged, 80 and over; Biomarkers; Case-Control Studies; Cohort Studies; Enzyme-Linked Immunosorbent Assay; Fibrinogen; Frail Elderly; Gait; Geriatric Assessment; Hand Strength; Haptoglobins; Humans; Interleukin-6; Motor Activity; Syndrome; Transferrin	2014
Clinical utility of malnutrition-inflammation score in maintenance hemodialysis patients: focus on identifying the best cut-off point. American journal of nephrology, 2008, Volume: 28, Issue:5 Topics: Adult; Aged; Aged, 80 and over; Alkaline Phosphatase; Female; Ferritins; Humans; Inflammation; Iron-Binding Proteins; Male; Malnutrition; Middle Aged; Renal Dialysis; Syndrome; Transferrin	2008
[CDG (congenital disorders of glycosylation). Differential hereditary ataxia in adulthood diagnosis]. Der Nervenarzt, 2002, Volume: 73, Issue:8 Topics: Adult; Brain; Brain Diseases, Metabolic, Inborn; Congenital Disorders of Glycosylation; Diagnosis, Differential; Female; Follow-Up Studies; Humans; Intellectual Disability; Isoelectric Focusing; Magnetic Resonance Imaging; Neuropsychological Tests; Spinocerebellar Degenerations; Syndrome; Transferrin	2002
Hereditary hyperferritinemia-cataract syndrome: a novel mutation in the iron-responsive element of the L-ferritin gene in a French family. The American journal of medicine, 2004, Jul-15, Volume: 117, Issue:2 Topics: Adult; Apoferritins; Cataract; Family Health; Female; Ferritins; Genetic Predisposition to Disease; Humans; Iron; Iron-Regulatory Proteins; Pedigree; Point Mutation; Syndrome; Transferrin	2004
Defective protein glycosylation in patients with cutis laxa syndrome. European journal of human genetics : EJHG, 2005, Volume: 13, Issue:4 Topics: Apolipoproteins C; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Consanguinity; Cutis Laxa; Extracellular Matrix Proteins; Female; Glycosylation; Humans; Infant, Newborn; Isoelectric Focusing; Male; Mutation; Pedigree; Polysaccharides; Recombinant Proteins; Syndrome; Transferrin	2005
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia. European journal of human genetics : EJHG, 2007, Volume: 15, Issue:6 Topics: Abnormalities, Multiple; Adaptor Proteins, Vesicular Transport; Apolipoprotein C-III; Carbohydrate Metabolism, Inborn Errors; Failure to Thrive; Fatal Outcome; Female; Glycosylation; Golgi Apparatus; Humans; Infant; Infant, Newborn; Isoelectric Focusing; Male; Microcephaly; Mutation; Syndrome; Thumb; Transferrin	2007
Implication of iron in seizure syndrome of mutant chicks (Gallus domesticus). Comparative biochemistry and physiology. A, Comparative physiology, 1983, Volume: 74, Issue:2 Topics: Animals; Blood Proteins; Brain; Chickens; Hemoglobins; Iron; Male; Mutation; Seizures; Syndrome; Transferrin	1983
[Serum protein fractions in patients with dyscirculatory encephalopathy in atherosclerosis and hypertension]. Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1984, Volume: 84, Issue:1 Topics: Adult; Aged; Blood Proteins; Cerebrovascular Disorders; Female; Haptoglobins; Humans; Hypertension; Intracranial Arteriosclerosis; Lipoproteins; Male; Middle Aged; Serum Albumin; Syndrome; Transferrin	1984
[Bureau-Barrière's acro-neuropathy. Complementary studies and definition of ante-acropathy status (author's transl)]. Annales de dermatologie et de venereologie, 1982, Volume: 109, Issue:3 Topics: Extremities; Humans; Immunoglobulin A; Nervous System Diseases; Radionuclide Imaging; Syndrome; Transferrin	1982
[Genetic markers of atypical phasic psychoses]. Psychiatria clinica, 1980, Volume: 13, Issue:1 Topics: Adult; Anxiety; Bipolar Disorder; Blood Proteins; Female; Haptoglobins; Humans; Male; Paranoid Disorders; Psychotic Disorders; Schizophrenia; Syndrome; Transferrin	1980
Failure to diagnose carbohydrate-deficient glycoprotein syndrome prenatally. Pediatric neurology, 1994, Volume: 11, Issue:1 Topics: alpha-Fetoproteins; Chorionic Villi Sampling; Diseases in Twins; Failure to Thrive; Glycoproteins; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Predictive Value of Tests; Prenatal Diagnosis; Syndrome; Transferrin	1994
Carbohydrate deficient glycoprotein syndrome; multiple abnormalities and diagnostic delay. Archives of disease in childhood, 1995, Volume: 72, Issue:5 Topics: Abnormalities, Multiple; Carbohydrate Metabolism, Inborn Errors; Deafness; Glycoproteins; Humans; Infant, Newborn; Male; Nephrotic Syndrome; Syndrome; Thyroid Gland; Transferrin	1995
Concerning "Agamanolis disease". American journal of medical genetics, 1995, Apr-10, Volume: 56, Issue:3 Topics: Carbohydrate Metabolism, Inborn Errors; Cholesterol; Glycoproteins; Glycosylation; Humans; Lipid Metabolism, Inborn Errors; Syndrome; Transferrin	1995
Normal N-oligosaccharyltransferase activity in fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome. Journal of inherited metabolic disease, 1994, Volume: 17, Issue:5 Topics: Amino Acid Sequence; Carbohydrates; Fibroblasts; Hexosyltransferases; Humans; Membrane Proteins; Molecular Sequence Data; Syndrome; Transferases; Transferrin	1994
Carbohydrate-deficient glycoprotein syndrome: not an N-linked oligosaccharide processing defect, but an abnormality in lipid-linked oligosaccharide biosynthesis? The Journal of clinical investigation, 1994, Volume: 94, Issue:5 Topics: Blood Proteins; Carbohydrates; Cell Line; Female; Glycoproteins; Glycosylation; Humans; Isoelectric Focusing; Lipid Metabolism; Mannose; Oligosaccharides; Syndrome; Transferrin	1994
[The iron overload syndrome in patients with severe bacterial inflammatory diseases and convalescents]. Gematologiia i transfuziologiia, 1993, Volume: 38, Issue:3 Topics: Acute Disease; Bacterial Infections; Child, Preschool; Convalescence; Ferritins; Humans; Infant; Iron; Meningoencephalitis; Pneumonia; Sepsis; Syndrome; Transferrin	1993
Diagnosis of carbohydrate-deficient glycoprotein syndrome by matrix-assisted laser desorption time-of-flight mass spectrometry. Biological mass spectrometry, 1994, Volume: 23, Issue:2 Topics: Carbohydrate Metabolism, Inborn Errors; Glycoproteins; Humans; Mass Spectrometry; Sialic Acids; Syndrome; Transferrin	1994
Electrospray ionization-mass spectrometric analysis of serum transferrin isoforms in patients with carbohydrate-deficient glycoprotein syndrome. Journal of biochemistry, 1993, Volume: 114, Issue:6 Topics: Amino Acid Sequence; Carbohydrate Metabolism, Inborn Errors; Carbohydrate Sequence; Glycopeptides; Glycoproteins; Humans; Isomerism; Mass Spectrometry; Molecular Sequence Data; Molecular Weight; Syndrome; Transferrin	1993
Early manifestations of the carbohydrate-deficient glycoprotein syndrome. The Journal of pediatrics, 1993, Volume: 122, Issue:1 Topics: Biomarkers; Carbohydrate Metabolism, Inborn Errors; Cerebellum; Failure to Thrive; Female; Glycoproteins; Humans; Infant; Male; Psychomotor Disorders; Syndrome; Transferrin	1993
Sugar chains of serum transferrin from patients with carbohydrate deficient glycoprotein syndrome. Evidence of asparagine-N-linked oligosaccharide transfer deficiency. The Journal of biological chemistry, 1993, Mar-15, Volume: 268, Issue:8 Topics: Asparagine; Carbohydrate Metabolism, Inborn Errors; Carbohydrate Sequence; Carbohydrates; Chromatography, Affinity; Chromatography, Gel; Electrophoresis, Polyacrylamide Gel; Humans; Isoelectric Point; Lectins; Metabolism, Inborn Errors; Molecular Sequence Data; Oligosaccharides; Syndrome; Transferrin	1993
Diagnosis of the carbohydrate-deficient glycoprotein syndrome by analysis of transferrin in filter paper blood spots. Acta paediatrica (Oslo, Norway : 1992), 1993, Volume: 82, Issue:1 Topics: Blood Specimen Collection; Carbohydrate Metabolism, Inborn Errors; Female; Glycoproteins; Humans; Infant, Newborn; Isoelectric Focusing; Male; Syndrome; Transferrin	1993
Renal cysts in the carbohydrate-deficient glycoprotein syndrome. Pediatric nephrology (Berlin, Germany), 1993, Volume: 7, Issue:3 Topics: Biomarkers; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Glycoproteins; Humans; Infant; Kidney Diseases, Cystic; Kidney Medulla; Male; Syndrome; Transferrin; Ultrasonography	1993
A new syndrome of liver iron overload with normal transferrin saturation. Lancet (London, England), 1997, Jan-11, Volume: 349, Issue:9045 Topics: Adolescent; Adult; Aged; Female; Hemochromatosis; HLA Antigens; HLA-A3 Antigen; Humans; Iron Overload; Liver; Male; Middle Aged; Syndrome; Transferrin	1997
Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy. The Journal of clinical investigation, 1998, Apr-01, Volume: 101, Issue:7 Topics: Cells, Cultured; Glycoproteins; Glycosylation; Humans; Infant; Male; Mannose; Mannose-6-Phosphate Isomerase; Mutation; Protein Processing, Post-Translational; Protein-Losing Enteropathies; Syndrome; Transferrin	1998
Insulin resistance, iron, and the liver. Lancet (London, England), 2000, Jun-24, Volume: 355, Issue:9222 Topics: Body Mass Index; Fatty Liver; Hemochromatosis; HLA-A3 Antigen; Humans; Hyperinsulinism; Hyperlipidemias; Insulin Resistance; Iron; Iron Overload; Liver; Liver Diseases; Obesity; Point Mutation; Syndrome; Transferrin	2000
Serum glycoproteins in autoimmune diseases. Acta medica Academiae Scientiarum Hungaricae, 1976, Volume: 33, Issue:2 Topics: Adult; Aged; alpha-Macroglobulins; Arthritis; Autoimmune Diseases; Beta-Globulins; Ceruloplasmin; Female; Glycoproteins; Hemopexin; Humans; Immunoglobulins; Lupus Erythematosus, Systemic; Male; Middle Aged; Orosomucoid; Syndrome; Transferrin	1976
[Changes in serum iron, total iron-binding capacity and cytological indices in pregnant women with an anemic syndrome]. Akusherstvo i ginekologiia, 1979, Volume: 18, Issue:3 Topics: Anemia, Hypochromic; Blood Cell Count; Female; Humans; Iron; Pregnancy; Pregnancy Complications, Hematologic; Protein Binding; Syndrome; Thalassemia; Transferrin	1979
Structure of serum transferrin in carbohydrate-deficient glycoprotein syndrome. Biochemical and biophysical research communications, 1992, Dec-15, Volume: 189, Issue:2 Topics: Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Affinity; Chromatography, High Pressure Liquid; Female; Glycosylation; Humans; Male; Mass Spectrometry; Molecular Weight; Sialic Acids; Syndrome; Transferrin	1992
The carbohydrate deficient glycoprotein syndrome in three Japanese children. Brain & development, 1992, Volume: 14, Issue:1 Topics: Adolescent; alpha 1-Antitrypsin; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Female; Glycoproteins; Humans; Isoelectric Focusing; Japan; Male; Phenotype; Syndrome; Transferrin	1992
Multiple serum protein abnormalities in carbohydrate-deficient glycoprotein syndrome: pathognomonic finding of two-dimensional electrophoresis? Clinical chemistry, 1992, Volume: 38, Issue:7 Topics: Adult; Carbohydrate Metabolism, Inborn Errors; Carbohydrates; Child, Preschool; Electrophoresis, Gel, Two-Dimensional; Female; Glycoproteins; Humans; Male; Syndrome; Transferrin	1992
Ocular pathology in disialotransferrin developmental deficiency syndrome. Ophthalmic paediatrics and genetics, 1990, Volume: 11, Issue:4 Topics: Adolescent; Adult; Child; Child, Preschool; Developmental Disabilities; Electroretinography; Esotropia; Female; Humans; Male; Motor Neurons; Neuromuscular Diseases; Retinitis Pigmentosa; Syndrome; Transferrin; Vision Disorders	1990
Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome. Archives of disease in childhood, 1991, Volume: 66, Issue:9 Topics: Bile Ducts; Carbohydrate Metabolism, Inborn Errors; Cerebellum; Glycoproteins; Humans; Infant, Newborn; Isoelectric Focusing; Kidney; Liver; Male; Olivopontocerebellar Atrophies; Sialic Acids; Syndrome; Transferrin	1991
[The carbohydrate deficient glycoprotein syndrome]. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1991, Apr-20, Volume: 111, Issue:10 Topics: Abnormalities, Multiple; Biomarkers; Brain; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Glycoproteins; Humans; Intellectual Disability; Male; Nervous System Diseases; Syndrome; Transferrin	1991
Carbohydrate deficient serum transferrin in a new systemic hereditary syndrome. Archives of disease in childhood, 1990, Volume: 65, Issue:1 Topics: Biomarkers; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Growth Disorders; Humans; Isoelectric Focusing; Nervous System Diseases; Syndrome; Transferrin	1990
Disialotransferrin developmental deficiency syndrome. Archives of disease in childhood, 1989, Volume: 64, Issue:1 Topics: Adolescent; Adult; Asialoglycoproteins; Child; Child, Preschool; Developmental Disabilities; Facial Expression; Female; Humans; Intellectual Disability; Isoelectric Focusing; Male; Metabolism, Inborn Errors; Nervous System Diseases; Sialoglycoproteins; Syndrome; Transferrin	1989
Disialotransferrin developmental deficiency syndrome and olivopontocerebellar atrophy. Archives of disease in childhood, 1989, Volume: 64, Issue:5 Topics: Adolescent; Adult; Child; Child, Preschool; Developmental Disabilities; Humans; Metabolism, Inborn Errors; Olivopontocerebellar Atrophies; Sialic Acids; Spinocerebellar Degenerations; Syndrome; Transferrin	1989
Serum iron status in Rett syndrome. Brain & development, 1987, Volume: 9, Issue:5 Topics: Adolescent; Adult; Age Factors; Brain Chemistry; Brain Diseases; Child; Child, Preschool; Female; Ferritins; Humans; Infant; Intellectual Disability; Iron; Syndrome; Transferrin	1987
Possible linkage between the loci for the trichodentoosseous (TDO) syndrome and the ABO blood group system: genetic and clinical implications. Birth defects original article series, 1974, Volume: 10, Issue:10 Topics: ABO Blood-Group System; Acid Phosphatase; Aminohydrolases; Bone and Bones; Dental Enamel Hypoplasia; Face; Genes, Dominant; Hair; Haptoglobins; Hemoglobins; Humans; Lewis Blood Group Antigens; Pedigree; Phosphoglucomutase; Phosphogluconate Dehydrogenase; Phosphotransferases; Rh-Hr Blood-Group System; Syndrome; Transferrin	1974
[Ferrokinetic studies in hemoglobin-Vienna hemoglobinopathy]. Acta medica Austriaca, 1974, Volume: 2, Issue:1 Topics: Acid Phosphatase; Adult; Bone Marrow; Erythrocytes; Hematocrit; Hemoglobinopathies; Hemoglobins, Abnormal; Hemolysis; Humans; Iron; Iron Radioisotopes; Male; Syndrome; Transferrin	1974
The potential pathogenic role of complement in dengue hemorrhagic shock syndrome. The New England journal of medicine, 1973, Nov-08, Volume: 289, Issue:19 Topics: Blood Proteins; Complement System Proteins; Dengue; Disseminated Intravascular Coagulation; Fibrin; Fibrinogen; Hemorrhagic Fevers, Viral; Humans; Shock; Syndrome; Thailand; Thrombocytopenia; Transferrin	1973
Syndromes of iron overload. Clinical toxicology, 1971, Volume: 4, Issue:4 Topics: Alcoholism; Anemia, Hemolytic; Erythropoiesis; Extremities; Folic Acid Deficiency; Hand Deformities, Acquired; Hemochromatosis; Hemosiderosis; Humans; Infant, Newborn; Intestinal Mucosa; Iron; Joint Diseases; Kinetics; Liver Cirrhosis; Osteochondritis; Siderosis; Spinal Diseases; Syndrome; Transferrin; Transfusion Reaction; Vitamin B 6 Deficiency	1971