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A clinical, pathological, and genetic characterization of methotrexate-associated lymphoproliferative disorders.

Published in The Journal of rheumatology

Our data demonstrate that patients in the EBVMCU, a specific clinical subgroup of MTX-LPD, had a better clinical outcome when MTX was withdrawn than did other patients with MTX-LPD.

Corneal opacities in the Hallermann-Streiff syndrome.

Published in Ophthalmic genetics

We present six patients with typical Hallermann-Streiff syndrome. All have microphthalmia and were operated for congenital cataract. Three of the patients developed a severe glaucoma and one patient presented repeated uveal effusions. Five of our patients have the same pattern of corneal stromal opacities. The opacities are ill defined and bilatera...

FAMILIAL RETICULOENDOTHELIOSIS WITH EOSINOPHILIA.

Published in The New England journal of medicine

INCIDENCE OF REACTIONS FOLLOWING ADMINISTRATION OF ANTIRABIES SERUM; STUDY OF 526 CASES.

Published in JAMA

WERNER'S SYNDROME.

Published in Annals of internal medicine

LIVEDO RETICULARIS IN ASSOCIATION WITH ACUTE LYMPHOCYTIC LEUKEMIA.

Published in Archives of dermatology

UNUSUAL CUTANEOUS FINDINGS IN PRIMARY SYSTEMIC AMYLOIDOSIS; REPORT OF A CASE.

Published in Archives of dermatology

PSORIASIS AND REITER'S SYNDROME.

Published in Archives of dermatology

A DEFICIENCY STATE ARISING IN INFANTS ON SYNTHETIC FOODS.

Published in Archives of disease in childhood

KERATOSES, CANCER AND "THE SIGN OF LESER-TR'ELAT".

Published in Cancer