Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S W Eber

Showing results (21-30 of 47) with videos related to

Pageof 5
Sort By:
Clinical Genetics|October 1, 1991
Saethre-Chotzen syndrome (ACS III) in four generationsS C Niemann-Seyde, S W Eber, B Zoll
Blut|July 1, 1986
Clinical symptoms and biochemical properties of three new glucosephosphate isomerase variantsS W Eber, M Gahr, M Lakomek, et al.
The Journal of Clinical Investigation|February 1, 1988
Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chainsS W Eber, S A Morris, W Schröter, et al.
Acta Neuropathologica|January 1, 1987
Neuropathology of Seckel syndrome in fetal stage with evidence of intrauterine developmental retardationA Hori, K Tamagawa, S W Eber, et al.
Laryngo- Rhino- Otologie|September 17, 1999
[Postoperative antibiotic therapy of cervical lymphadenitis caused by nontuberculous, atypical mycobacteria]M C Jäckel, O Witt, S W Eber, et al.
Zeitschrift Fur Kinderchirurgie : Organ Der Deutschen, Der Schweizerischen Und Der Osterreichischen Gesellschaft Fur Kinderchirurgie = Surgery in Infancy and Childhood|October 1, 1986
[Corrective craniofacial surgery in the acrocephalosyndactylia syndrome (Saethre-Chotzen syndrome)]S W Eber, H G Luhr, O Spoerri, et al.
European Journal of Pediatrics|August 1, 1988
Glucuronyl transferase deficiency and mild hereditary spherocytosis: effect of splenectomyS W Eber, D Ullrich, C P Speer, et al.
Acta Haematologica|January 1, 1990
Combination of congenital nonspherocytic haemolytic anaemia and impairment of granulocyte function in severe glucosephosphate isomerase deficiency. A new variant enzyme designated GPI CaldenB A Neubauer, S W Eber, M Lakomek, et al.
International Journal of Hematology|April 4, 2000
Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese populationY Yawata, A Kanzaki, A Yawata, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1993
[Hemolytic-uremic syndrome in pneumococcal meningitis and infection. Importance of T-transformation]S W Eber, H Polster, S H Quentin, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Clinical Genetics|October 1, 1991
Saethre-Chotzen syndrome (ACS III) in four generationsS C Niemann-Seyde, S W Eber, B Zoll
Blut|July 1, 1986
Clinical symptoms and biochemical properties of three new glucosephosphate isomerase variantsS W Eber, M Gahr, M Lakomek, et al.
The Journal of Clinical Investigation|February 1, 1988
Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chainsS W Eber, S A Morris, W Schröter, et al.
Acta Neuropathologica|January 1, 1987
Neuropathology of Seckel syndrome in fetal stage with evidence of intrauterine developmental retardationA Hori, K Tamagawa, S W Eber, et al.
Laryngo- Rhino- Otologie|September 17, 1999
[Postoperative antibiotic therapy of cervical lymphadenitis caused by nontuberculous, atypical mycobacteria]M C Jäckel, O Witt, S W Eber, et al.
Zeitschrift Fur Kinderchirurgie : Organ Der Deutschen, Der Schweizerischen Und Der Osterreichischen Gesellschaft Fur Kinderchirurgie = Surgery in Infancy and Childhood|October 1, 1986
[Corrective craniofacial surgery in the acrocephalosyndactylia syndrome (Saethre-Chotzen syndrome)]S W Eber, H G Luhr, O Spoerri, et al.
European Journal of Pediatrics|August 1, 1988
Glucuronyl transferase deficiency and mild hereditary spherocytosis: effect of splenectomyS W Eber, D Ullrich, C P Speer, et al.
Acta Haematologica|January 1, 1990
Combination of congenital nonspherocytic haemolytic anaemia and impairment of granulocyte function in severe glucosephosphate isomerase deficiency. A new variant enzyme designated GPI CaldenB A Neubauer, S W Eber, M Lakomek, et al.
International Journal of Hematology|April 4, 2000
Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese populationY Yawata, A Kanzaki, A Yawata, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1993
[Hemolytic-uremic syndrome in pneumococcal meningitis and infection. Importance of T-transformation]S W Eber, H Polster, S H Quentin, et al.
Pageof 5