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biotin and Antibody Deficiency Syndrome

biotin has been researched along with Antibody Deficiency Syndrome in 14 studies

Research

Studies (14)

Timeframe	Studies, this research(%)	All Research%
pre-1990	14 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
CHIARI, G	1
PETROVIC, C; VUJASIN, J	1
TASOVAC, B	1
DEBERNARDI, P; PETROCINI, S	1
NISENSON, A	1
BARIL, E; DAGENAIS-PERUSSE, P; HAZARD, E; OUADAHI, S	1
SVEJCAR, J	1
MARTIN, C	1
KRYSTIK, F	1
Charpentier, C; Coudé, FX; Dray, F; Fischer, A; Frézal, J; Griscelli, C; Mamas, S; Munnich, A; Saudubray, JM	1
Amman, AJ; Cowan, MJ; Malamud, N; Packman, S; Sander, JE; Wara, DW	1
Ammann, AJ; Cowan, MJ; Nyhan, W; Packman, S; Sweetman, L; Wara, DW; Yoshino, M	1
Williams, ML	1

Reviews

2 review(s) available for biotin and Antibody Deficiency Syndrome

Article	Year
Multiple biotin-dependent carboxylase deficiencies associated with defects in immunity. Nutrition reviews, 1979, Volume: 37, Issue:9 Topics: Apoenzymes; Biotin; Candidiasis, Cutaneous; Carboxy-Lyases; Female; Humans; Immunity, Cellular; Immunologic Deficiency Syndromes; Infant; Metabolism, Inborn Errors	1979
Biotin-responsive multiple carboxylase deficiency and immunodeficiency. Current problems in dermatology, 1989, Volume: 18 Topics: Amidohydrolases; Biotin; Biotinidase; Carboxy-Lyases; Humans; Immunologic Deficiency Syndromes; Metabolism, Inborn Errors	1989

Other Studies

12 other study(ies) available for biotin and Antibody Deficiency Syndrome

Article	Year
[Blood level of biotin in seborrheic dermatitis, Leiner's disease and eczema in infants]. Bollettino della Societa italiana di biologia sperimentale, 1952, Volume: 28, Issue:7 Topics: Biotin; Blood; Complement C5; Dermatitis, Exfoliative; Dermatitis, Seborrheic; Eczema; Hereditary Complement Deficiency Diseases; Humans; Immunologic Deficiency Syndromes; Infant	1952
Biotin in some erythemato-squamous dermatoses of babies. Dermatologica, 1952, Volume: 105, Issue:3 Topics: Biotin; Complement C5; Dermatitis, Exfoliative; Dermatitis, Seborrheic; Hereditary Complement Deficiency Diseases; Humans; Immunologic Deficiency Syndromes; Infant; Skin Diseases	1952
[Therapy of Leiner's disease with biotin]. Srpski arhiv za celokupno lekarstvo, 1954, Volume: 82, Issue:2 Topics: Biotin; Complement C5; Dermatitis, Exfoliative; Hereditary Complement Deficiency Diseases; Immunologic Deficiency Syndromes	1954
[Biotin in the treatment of desquamating erythroderma and seborrheic dermatitis: clinical results]. Il Lattante, 1954, Volume: 25, Issue:6 Topics: Biotin; Child; Complement C5; Dermatitis, Exfoliative; Dermatitis, Seborrheic; Hereditary Complement Deficiency Diseases; Humans; Immunologic Deficiency Syndromes; Infant	1954
Seborrheic dermatitis of infants and Leiners's disease: a biotin deficiency. The Journal of pediatrics, 1957, Volume: 51, Issue:5 Topics: Biotin; Biotinidase Deficiency; Child; Complement C5; Dermatitis, Exfoliative; Dermatitis, Seborrheic; Hereditary Complement Deficiency Diseases; Humans; Immunologic Deficiency Syndromes; Infant	1957
[The use of biotin in Leiner-Moussus disease]. L'union medicale du Canada, 1961, Volume: 90 Topics: Biotin; Complement C5; Dermatitis, Exfoliative; Hereditary Complement Deficiency Diseases; Humans; Immunologic Deficiency Syndromes	1961
[Correlation between biotin and certain dermatoses in newborn]. Casopis lekaru ceskych, 1950, Dec-01, Volume: 89, Issue:48 Topics: Biotin; Complement C5; Dermatitis, Exfoliative; Hereditary Complement Deficiency Diseases; Humans; Immunologic Deficiency Syndromes; Infant; Infant, Newborn; Skin Diseases	1950
[Treatment of erythroderma desquamativa by biotin]. Archives francaises de pediatrie, 1951, Volume: 8, Issue:3 Topics: Biotin; Complement C5; Dermatitis, Exfoliative; Folic Acid; Hereditary Complement Deficiency Diseases; Immunologic Deficiency Syndromes; Vitamin B Complex	1951
[Leiner-Moussous erythroderma desquamativa and biotin]. Lekarske listy, 1951, Nov-15, Volume: 6, Issue:22 Topics: Biotin; Complement C5; Dermatitis, Exfoliative; Hereditary Complement Deficiency Diseases; Humans; Immunologic Deficiency Syndromes	1951
Biotin-responsive immunoregulatory dysfunction in multiple carboxylase deficiency. Journal of clinical immunology, 1982, Volume: 2, Issue:1 Topics: Biotin; Carboxy-Lyases; Concanavalin A; Dinoprostone; Humans; Immunity, Cellular; Immunologic Deficiency Syndromes; Infant; Lymphocyte Activation; Male; Monocytes; Prostaglandins E; T-Lymphocytes, Regulatory	1982
Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies: a biotin-responsive disorder. Annals of neurology, 1980, Volume: 8, Issue:5 Topics: Biotin; Carboxy-Lyases; Cerebellar Ataxia; Cerebellum; Child, Preschool; Female; Humans; Immunologic Deficiency Syndromes; Infant; Male	1980
Multiple biotin-dependent carboxylase deficiencies associated with defects in T-cell and B-cell immunity. Lancet (London, England), 1979, Jul-21, Volume: 2, Issue:8134 Topics: Alopecia; B-Lymphocytes; Biotin; Candidiasis, Cutaneous; Carboxy-Lyases; Cerebellar Ataxia; Child, Preschool; Female; Humans; Immunologic Deficiency Syndromes; Infant; Keratoconjunctivitis; Male; Metabolism, Inborn Errors; T-Lymphocytes	1979