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Showing results (11-20 of 16) with videos related to

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Journal of Perinatal Medicine|January 1, 1996
Acute intermittent porphyria first diagnosed in the third trimester of pregnancy. Case reportD Soriano, D S Seidman, S Mashiach, et al.
Israel Journal of Medical Sciences|June 1, 1985
Malignant phenylketonuria due to defective synthesis of dihydrobiopterinB E Cohen, A Szeinberg, J Quint, et al.
AJR. American Journal of Roentgenology|January 1, 1983
Multiple endocrine neoplasia (MEN) syndrome type IIB: gastrointestinal manifestationsT C Demos, J Blonder, W L Schey, et al.
Vaccine|December 12, 2001
ProJuvant (Pluronic F127/chitosan) enhances the immune response to intranasally administered tetanus toxoidM A Westerink, S L Smithson, N Srivastava, et al.
Israel Journal of Medical Sciences|September 1, 1973
Dubin-Johnson Syndrome. Abnormal excretion of the isomers of urinary coproporphyrin by clinically unaffected family membersJ Ben-Ezzer, J Blonder, M Shani, et al.
Nephron|January 1, 1993
Hyperoxaluria is not a cause of nephrocalcinosis in phosphate-treated patients with hereditary hypophosphatemic ricketsM Tieder, J Blonder, S Strauss, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Journal of Perinatal Medicine|January 1, 1996
Acute intermittent porphyria first diagnosed in the third trimester of pregnancy. Case reportD Soriano, D S Seidman, S Mashiach, et al.
Israel Journal of Medical Sciences|June 1, 1985
Malignant phenylketonuria due to defective synthesis of dihydrobiopterinB E Cohen, A Szeinberg, J Quint, et al.
AJR. American Journal of Roentgenology|January 1, 1983
Multiple endocrine neoplasia (MEN) syndrome type IIB: gastrointestinal manifestationsT C Demos, J Blonder, W L Schey, et al.
Vaccine|December 12, 2001
ProJuvant (Pluronic F127/chitosan) enhances the immune response to intranasally administered tetanus toxoidM A Westerink, S L Smithson, N Srivastava, et al.
Israel Journal of Medical Sciences|September 1, 1973
Dubin-Johnson Syndrome. Abnormal excretion of the isomers of urinary coproporphyrin by clinically unaffected family membersJ Ben-Ezzer, J Blonder, M Shani, et al.
Nephron|January 1, 1993
Hyperoxaluria is not a cause of nephrocalcinosis in phosphate-treated patients with hereditary hypophosphatemic ricketsM Tieder, J Blonder, S Strauss, et al.
Pageof 2