Biomedical subjects
J Abulafia
Publications and source records attributed to J Abulafia.
[Melkersson-Rosenthal's syndrome. Its relation to Miescher granulomatous macrocheilia and Bernier-Boeck-Schaumann disease].
Explore the source record for details and available documents.
[Subcutaneous idiopathic fribomatosis(fascitis type). Combined with idiopathic mediastinal firosis and Riedel's struma(analysis of a general classification of fibromatous hyperplasias)].
Explore the source record for details and available documents.
[Histiocytosis-X. Developmental disparity of 2 observations in early infancy. Relations with "disseminated benign reticulosis in the child's skin"].
Explore the source record for details and available documents.
[Contribution to the etiopathogenicity of subcorneal pustular dermatosis (Sneddon and Wilkinson)].
Explore the source record for details and available documents.
[Circumscribed sclerodermatrophic syndrome].
Explore the source record for details and available documents.
[Malignant atrophic papulosis (Degos). (Fatal cutaneo-intestinal syndrome. Disseminated cutaneo-intestinal thromboangiitis)].
Explore the source record for details and available documents.
[Chronic myeloid leukemia with a dermatologic picture of erythema elevatum et diutinum].
Explore the source record for details and available documents.
[Primary cutaneous amyloidosis].
Explore the source record for details and available documents.
[Lymphocytic lymphoma associated with alopecia mucinosa].
Explore the source record for details and available documents.
[Peladoid erythematous lupus of the scalp].
Explore the source record for details and available documents.
[Cystic and nodular elastosis with comedos (Favre and Racouchot disease) and bullous and erosive porphyria in adults].
Explore the source record for details and available documents.
Van der Woude syndrome. A case report.
We describe several members of a family with Van der Woude syndrome, a genetic and congenital malformation syndrome with autosomal dominant inheritance and 70% to 80% penetrance with variable expressivity. It is characterized by clinical signs localized to the face, such as bilateral or unilateral pits on conical elevations in babies or extensive depressions in adults, both in the vermilion border of the lower lip, with cleft lip, with or without cleft palate and uvula. Small accessory or heterotopic salivary glands empty into sinuses or fistulas in the lips. This eight member family had various clinical signs of the condition. All had cleft lip and palate. We studied the major characteristics of the eight patients and describe histopathologic and immunohistochemical features.