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D Russo

Showing results (241-250 of 446) with videos related to

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European Journal of Neurology|December 31, 2013
Expression of vesicle-associated membrane-protein-associated protein B cleavage products in peripheral blood leukocytes and cerebrospinal fluid of patients with sporadic amyotrophic lateral sclerosisI Deidda, G Galizzi, R Passantino, et al.
Infocare : Information Strategies for Healthcare Networks|August 6, 1994
Verifying the future of electronic eligibility verificationJ R Stevens, K O'Donnell, D Russo, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|January 25, 2019
Protein-Polymer Dynamics as Affected by Polymer Coating and InteractionsD Russo, A De Angelis, A Paciaroni, et al.
Nephron|January 1, 1988
Treatment of severe renovascular hypertension by percutaneous transluminal renal angioplasty in patients with solitary functioning kidney. Effects on blood pressure and renal functionD Russo, V Iaccarino, G Conte, et al.
Neuro-Chirurgie|March 6, 2021
A choroid plexus metastasis of a prostatic adenocarcinoma mimicking a choroid plexus carcinoma: A case reportA Sellier, D Russo, F C Robertson, et al.
Minerva Nefrologica|July 1, 1981
[Glomerular dynamics in pregnancy. Study by micropuncture in rats]A Dal Canton, G Conte, C Esposito, et al.
British Journal of Haematology|August 12, 1999
Liposome-encapsulated daunorubicin for PGP-related multidrug resistanceM Michieli, D Damiani, A Ermacora, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|March 31, 2001
A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTCE Chiefari, R Chiarella, U Crocetti, et al.
Journal of Endocrinological Investigation|March 10, 2005
Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristicsD Scarpelli, L D'Aloiso, F Arturi, et al.
Journal of Endocrinological Investigation|September 21, 2002
Similarities and differences in the phenotype of members of an Italian family with hereditary non-autoimmune hyperthyroidism associated with an activating TSH receptor germline mutationF Arturi, E Chiefari, S Tumino, et al.
Pageof 45

Showing results (241-250 of 446) with videos related to

Sort By:
Pageof 45
European Journal of Neurology|December 31, 2013
Expression of vesicle-associated membrane-protein-associated protein B cleavage products in peripheral blood leukocytes and cerebrospinal fluid of patients with sporadic amyotrophic lateral sclerosisI Deidda, G Galizzi, R Passantino, et al.
Infocare : Information Strategies for Healthcare Networks|August 6, 1994
Verifying the future of electronic eligibility verificationJ R Stevens, K O'Donnell, D Russo, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|January 25, 2019
Protein-Polymer Dynamics as Affected by Polymer Coating and InteractionsD Russo, A De Angelis, A Paciaroni, et al.
Nephron|January 1, 1988
Treatment of severe renovascular hypertension by percutaneous transluminal renal angioplasty in patients with solitary functioning kidney. Effects on blood pressure and renal functionD Russo, V Iaccarino, G Conte, et al.
Neuro-Chirurgie|March 6, 2021
A choroid plexus metastasis of a prostatic adenocarcinoma mimicking a choroid plexus carcinoma: A case reportA Sellier, D Russo, F C Robertson, et al.
Minerva Nefrologica|July 1, 1981
[Glomerular dynamics in pregnancy. Study by micropuncture in rats]A Dal Canton, G Conte, C Esposito, et al.
British Journal of Haematology|August 12, 1999
Liposome-encapsulated daunorubicin for PGP-related multidrug resistanceM Michieli, D Damiani, A Ermacora, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|March 31, 2001
A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTCE Chiefari, R Chiarella, U Crocetti, et al.
Journal of Endocrinological Investigation|March 10, 2005
Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristicsD Scarpelli, L D'Aloiso, F Arturi, et al.
Journal of Endocrinological Investigation|September 21, 2002
Similarities and differences in the phenotype of members of an Italian family with hereditary non-autoimmune hyperthyroidism associated with an activating TSH receptor germline mutationF Arturi, E Chiefari, S Tumino, et al.
Pageof 45