HLA type and occurrence of disease in familial polyglandular failure.

The polyglandular failure syndrome: disease inheritance, HLA type, and immune function.

Frequent occurrence of asplenism and cholelithiasis in patients with autoimmune polyglandular disease type I.

Familial occurrence of inflammatory bowel disease.

Immunogenetics of the polyglandular failure syndrome.

Familial occurrence of histiocytosis.

Familial occurrence of entrapment neuropathies.

Familial occurrence of infantile myofibromatosis.

Polyglandular autoimmune syndrome type II in patients with idiopathic Addison's disease.

Hutchinson-Gilford progeria: familial occurrence.

Addison's disease in a patient with hypothyroidism: autoimmune polyglandular syndrome type 2.

Type 1 diabetes and polyglandular autoimmune syndrome: A review.

Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy.

Familial rheumatoid arthritis and HLA-DRw4.

Co-occurrence of type 1 diabetes mellitus and celiac disease.

HLA-DR1 in familial frontal fibrosing alopecia.

HLA typing in familial renal carcinoma.

HLA determinants in familial multiple sclerosis.

Apical hypertrophic cardiomyopathy of the Japanese type: occurrence with familial hypertrophic cardiomyopathy in a family.

Co-occurrence of Type 1 Diabetes and Celiac Disease Autoimmunity.

Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering.

Autoimmune polyglandular syndrome type 2: a rare condition in childhood.

Alopecia universalis in polyglandular autoimmune syndrome type I.

Alopecia universalis in autoimmune polyglandular syndrome type I.

Familial occurrence of chromosome variant 17ph+.

Suggest Documents

The polyglandular failure syndrome: disease inheritance, HLA type, and immune function.

Frequent occurrence of asplenism and cholelithiasis in patients with autoimmune polyglandular disease type I.

Familial occurrence of inflammatory bowel disease.

Immunogenetics of the polyglandular failure syndrome.

Familial occurrence of histiocytosis.

Familial occurrence of entrapment neuropathies.

Familial occurrence of infantile myofibromatosis.

Polyglandular autoimmune syndrome type II in patients with idiopathic Addison's disease.

Hutchinson-Gilford progeria: familial occurrence.

Addison's disease in a patient with hypothyroidism: autoimmune polyglandular syndrome type 2.

Type 1 diabetes and polyglandular autoimmune syndrome: A review.

Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy.

Familial rheumatoid arthritis and HLA-DRw4.

Co-occurrence of type 1 diabetes mellitus and celiac disease.

HLA-DR1 in familial frontal fibrosing alopecia.

HLA typing in familial renal carcinoma.

HLA determinants in familial multiple sclerosis.

Apical hypertrophic cardiomyopathy of the Japanese type: occurrence with familial hypertrophic cardiomyopathy in a family.

Co-occurrence of Type 1 Diabetes and Celiac Disease Autoimmunity.

Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering.

Autoimmune polyglandular syndrome type 2: a rare condition in childhood.

Alopecia universalis in polyglandular autoimmune syndrome type I.

Alopecia universalis in autoimmune polyglandular syndrome type I.

Familial occurrence of chromosome variant 17ph+.

HLA type and occurrence of disease in familial polyglandular failure.

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