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M Celli

Showing results (21-30 of 42) with videos related to

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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|April 3, 2010
Taurine deficiency in thalassemia major-induced osteoporosis treated with neridronateP D'Eufemia, R Finocchiaro, M Celli, et al.
Biochimica Et Biophysica Acta|February 16, 1999
Effect of D-ribose on purine synthesis and neurological symptoms in a patient with adenylosuccinase deficiencyC Salerno, P D'Eufemia, R Finocchiaro, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|September 4, 2017
Clinical and biochemical response to neridronate treatment in a patient with osteoporosis-pseudoglioma syndrome (OPPG)M Celli, P D'Eufemia, P Persiani, et al.
American Journal of Perinatology|September 30, 2000
Sandifer's syndrome in a breast-fed infantG Corrado, M Cavaliere, P D'Eufemia, et al.
Organic Letters|October 27, 2001
On the photoreactivity of 4,5-dithiophen-3-yl-[1,3]dithiol-2-one. The first preparation of a thieno[3,4-c]dithiineA M Celli, D Donati, F Ponticelli, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 1996
Abnormal intestinal permeability in children with autismP D'Eufemia, M Celli, R Finocchiaro, et al.
Cephalalgia : an International Journal of Headache|November 14, 1997
Erythrocyte and plasma levels of glutamate and aspartate in children affected by migraineP D'Eufemia, R Finocchiaro, D Lendvai, et al.
Clinical Chemistry|May 1, 1995
Rapid gas-chromatographic assay of lactulose and mannitol for estimating intestinal permeabilityM Celli, P D'Eufemia, R Dommarco, et al.
American Journal of Medical Genetics|September 15, 1992
Child with manifestations of dermotrichic syndrome and ichthyosis follicularis-alopecia-photophobia (IFAP) syndromeF Martino, P D'Eufemia, M S Pergola, et al.
Minerva Pediatrica|December 8, 1998
[Jejunal enteral feeding in a severe case of reflux esophagitis in an infant with Pierre-Robin syndrome]M Chiaretti, R M Fracassi, P Ferrante, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|April 3, 2010
Taurine deficiency in thalassemia major-induced osteoporosis treated with neridronateP D'Eufemia, R Finocchiaro, M Celli, et al.
Biochimica Et Biophysica Acta|February 16, 1999
Effect of D-ribose on purine synthesis and neurological symptoms in a patient with adenylosuccinase deficiencyC Salerno, P D'Eufemia, R Finocchiaro, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|September 4, 2017
Clinical and biochemical response to neridronate treatment in a patient with osteoporosis-pseudoglioma syndrome (OPPG)M Celli, P D'Eufemia, P Persiani, et al.
American Journal of Perinatology|September 30, 2000
Sandifer's syndrome in a breast-fed infantG Corrado, M Cavaliere, P D'Eufemia, et al.
Organic Letters|October 27, 2001
On the photoreactivity of 4,5-dithiophen-3-yl-[1,3]dithiol-2-one. The first preparation of a thieno[3,4-c]dithiineA M Celli, D Donati, F Ponticelli, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 1996
Abnormal intestinal permeability in children with autismP D'Eufemia, M Celli, R Finocchiaro, et al.
Cephalalgia : an International Journal of Headache|November 14, 1997
Erythrocyte and plasma levels of glutamate and aspartate in children affected by migraineP D'Eufemia, R Finocchiaro, D Lendvai, et al.
Clinical Chemistry|May 1, 1995
Rapid gas-chromatographic assay of lactulose and mannitol for estimating intestinal permeabilityM Celli, P D'Eufemia, R Dommarco, et al.
American Journal of Medical Genetics|September 15, 1992
Child with manifestations of dermotrichic syndrome and ichthyosis follicularis-alopecia-photophobia (IFAP) syndromeF Martino, P D'Eufemia, M S Pergola, et al.
Minerva Pediatrica|December 8, 1998
[Jejunal enteral feeding in a severe case of reflux esophagitis in an infant with Pierre-Robin syndrome]M Chiaretti, R M Fracassi, P Ferrante, et al.
Pageof 5