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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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L Moschini

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Annali Dell'Istituto Superiore Di Sanita|March 3, 1999

[Re-evaluation of the diagnosis in congenital hypothyroidism]P Costa, L Sambuco, A Olivieri, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1996

Intra-arterial thrombolysis in acute ischaemic stroke: experience with a superselective catheter embedded in the clotL Casto, L Caverni, M Camerlingo, et al.

Annali Dell'Istituto Superiore Di Sanita|January 1, 1991

[Congenital hypothyroidism: organization and coordination of neonatal screening in Italy]S Carta, M E Grandolfo, L Moschini, et al.

Journal of Endocrinological Investigation|January 1, 1982

Familial thyroxine-binding globulin deficiency detected in a pilot screening program for congenital hypothyroidismM Carta Sorcini, L Moschini, L Fiore, et al.

Helvetica Paediatrica Acta|December 1, 1986

Longitudinal assessment of children with congenital hypothyroidism detected by neonatal screeningL Moschini, P Costa, E Marinelli, et al.

Thyroid : Official Journal of the American Thyroid Association|June 1, 1997

Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesisP Lapi, P E Macchia, L Chiovato, et al.

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Search research articles

Showing results (31-40 of 36) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 36 results.

Annali Dell'Istituto Superiore Di Sanita|March 3, 1999

[Re-evaluation of the diagnosis in congenital hypothyroidism]P Costa, L Sambuco, A Olivieri, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1996

Intra-arterial thrombolysis in acute ischaemic stroke: experience with a superselective catheter embedded in the clotL Casto, L Caverni, M Camerlingo, et al.

Annali Dell'Istituto Superiore Di Sanita|January 1, 1991

[Congenital hypothyroidism: organization and coordination of neonatal screening in Italy]S Carta, M E Grandolfo, L Moschini, et al.

Journal of Endocrinological Investigation|January 1, 1982

Familial thyroxine-binding globulin deficiency detected in a pilot screening program for congenital hypothyroidismM Carta Sorcini, L Moschini, L Fiore, et al.

Helvetica Paediatrica Acta|December 1, 1986

Longitudinal assessment of children with congenital hypothyroidism detected by neonatal screeningL Moschini, P Costa, E Marinelli, et al.

Thyroid : Official Journal of the American Thyroid Association|June 1, 1997

Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesisP Lapi, P E Macchia, L Chiovato, et al.

Pageof 4