المؤلفون: Pavel, AM, O'Toole, JM, Proietti, J, Livingstone, V, Mitra, S, Marnane, WP, Finder, M, Dempsey, EM, Murray, DM, Boylan, GB, NSeR Consortium

المصدر: Epilepsia. 64(2):456-468

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:151441169

المؤلفون: Proietti, J., Nanyunja, C., Mathieson, S. R., Duckworth, E., Sadoo, S., Mambule, I., Nakimuli, A., Tann, C. J., Boylan, G. B.

المصدر: Epileptic Disorders ; ISSN 1294-9361 1950-6945

الاتاحة: http://dx.doi.org/10.1002/epd2.20299
https://onlinelibrary.wiley.com/doi/pdf/10.1002/epd2.20299

المؤلفون: Cossu, A, Lo Barco, T, Proietti, J, Dalla Bernardina, B, Cantalupo, G, Ghobert, L, Brambilla, I, Giarola, E, Costa, A, De Benito, T, Bethge, S, Cardot, S, Montwill, Iga, Remonato, E, Gramaglia, S, Darra, F

المساهمون: Cossu, A, Lo Barco, T, Proietti, J, Dalla Bernardina, B, Cantalupo, G, Ghobert, L, Brambilla, I, Giarola, E, Costa, A, De Benito, T, Bethge, S, Cardot, S, Montwill, Iga, Remonato, E, Gramaglia, S, Darra, F

مصطلحات موضوعية: Caregiver, Encephalopathy, Epilepsy, KCNQ2, Neonatal seizures, Outcome, Phenotype, Severity

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/36989566; info:eu-repo/semantics/altIdentifier/wos/WOS:000966711600001; volume:142; issue:109153; firstpage:1; lastpage:7; numberofpages:7; journal:EPILEPSY & BEHAVIOR; https://hdl.handle.net/11562/1091091; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85151416712

الاتاحة: https://hdl.handle.net/11562/1091091
https://doi.org/10.1016/j.yebeh.2023.109153

المؤلفون: Lo Barco, T, Ghobert, AL, Lucca, F, Galati, G, Proietti, J, Cantalupo, G

المساهمون: Lo Barco, T, Ghobert, Al, Lucca, F, Galati, G, Proietti, J, Cantalupo, G

Relation: info:eu-repo/semantics/altIdentifier/pmid/34246348; info:eu-repo/semantics/altIdentifier/wos/WOS:000671078800026; volume:398; issue:10295; firstpage:156; lastpage:156; journal:THE LANCET; http://hdl.handle.net/11380/1290169; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85110251515

الاتاحة: http://hdl.handle.net/11380/1290169
https://doi.org/10.1016/S0140-6736(21)01048-5

المؤلفون: Proietti J., Amadori E., Striano P., Ricci E., Cordelli D. M., Bana C., Dilena R., Gardella E., Klint Nielsen J. E., Pisani F., Lo Barco T., Fiorini E., Fontana E., Darra F., Dalla Bernardina B., Cantalupo G.

المساهمون: Proietti, J., Amadori, E., Striano, P., Ricci, E., Cordelli, D. M., Bana, C., Dilena, R., Gardella, E., Klint Nielsen, J. E., Pisani, F., Lo Barco, T., Fiorini, E., Fontana, E., Darra, F., Dalla Bernardina, B., Cantalupo, G.

مصطلحات موضوعية: ARID1B gene, Coffin-Siris Syndrome, Rolandic trait, childhood, fever susceptibility, focal epilepsy, DNA-Binding Protein, Face, Human, Neck, Transcription Factor, Abnormalities, Multiple, Epilepsy, Hand Deformities, Congenital, Intellectual Disability, Micrognathism

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/34730517; info:eu-repo/semantics/altIdentifier/wos/WOS:000734656900007; volume:23; firstpage:865; lastpage:874; numberofpages:10; journal:EPILEPTIC DISORDERS; http://hdl.handle.net/11567/1083295; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85122503778

الاتاحة: http://hdl.handle.net/11567/1083295
https://doi.org/10.1684/epd.2021.1356

المؤلفون: Manuck, Stephen B., Proietti, Oseph J.m., Rader, Sally J., Polefrone, Joanna M., Manuck, S B, Proietti, J M, Rader, S J, Polefrone, J M

المصدر: Psychosomatic Medicine; Mar/Apr1985, Vol. 47 Issue 2, p189-200, 12p

المؤلفون: Emilia Ricci, Francesca Darra, Jens Erik Klint Nielsen, Gaetano Cantalupo, Elena Fiorini, Elena Fontana, Elisabetta Amadori, Francesco Pisani, Bernardo Dalla Bernardina, Pasquale Striano, Tommaso Lo Barco, Robertino Dilena, Cristina Bana, Duccio Maria Cordelli, Elena Gardella, Jacopo Proietti

المساهمون: Proietti J., Amadori E., Striano P., Ricci E., Cordelli D.M., Bana C., Dilena R., Gardella E., Klint Nielsen J.E., Pisani F., Lo Barco T., Fiorini E., Fontana E., Darra F., Dalla Bernardina B., Cantalupo G.

مصطلحات موضوعية: focal epilepsy, Pediatrics, medicine.medical_specialty, Micrognathism, fever susceptibility, Congenital, Epilepsy, ARID1B gene, Coffin-Siris Syndrome, Rolandic trait, childhood, Intellectual Disability, medicine, otorhinolaryngologic diseases, Humans, Abnormalities, Multiple, Ictal, Congenital Malformation Syndrome, Coffin–Siris syndrome, Motor area, business.industry, Spike-and-wave, General Medicine, Hand Deformities, medicine.disease, DNA-Binding Proteins, Neurology, Face, EEG Findings, Neurology (clinical), Abnormalities, business, Multiple, Hand Deformities, Congenital, Developmental regression, Neck, Transcription Factors

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57c5df09b8f9cad9f0a520d4f41ed4a5
http://hdl.handle.net/11585/857165