Search Results - "Epifanio R"

High-dose recombinant LH add-back strategy using high-dose GnRH antagonist is an innovative protocol compared with standard GnRH antagonist.

Authors: Garcia-Velasco, J. A. Bennink, H. J. T. Coelingh Epifanio, R. et al.

Source: Reproductive BioMedicine Online (Reproductive Healthcare Limited). Feb2011 Supplement, Vol. 22 Issue S1, p280-287. 8p.

High-dose recombinant LH add-back strategy using high-dose GnRH antagonist is an innovative protocol compared with standard GnRH antagonist.

Authors: Garcia-Velasco, J. A. Bennink, H. J. T. Coelingh Epifanio, R. et al.

Source: Reproductive BioMedicine Online (Reproductive Healthcare Limited). Sep2007, Vol. 15 Issue 3, p280-287. 8p.

Urinary Human Chorionic Gonadotropin (hCG), Intramuscular or Subcutaneously Administered, Yields higher hCG Serum and Follicular Levels Than Recombinant hCG in Egg Donors.

Authors: Vidal, C. Zuzuaregui, J. Epifanio, R. et al.

Source: Fertility & Sterility. Sep2005 Supplement 1, Vol. 84, pS296-S297. 2p.

A mathematical equation to calculate the maximum pregnancy rate with a minimum risk for multiple pregnancies in patients undergoing IVF.

Authors: Rodriguez, Manuel Escudero, E. Epifanio, R. et al.

Source: Fertility & Sterility. 2003 Supplement 3, Vol. 80, p160-161. 2p.

Auditory attention at the onset of West syndrome: Correlation with EEG patterns and visual function

Authors: Baranello, G. Randò, T. Bancale, A. et al.

Source: Brain & Development. Jun2006, Vol. 28 Issue 5, p293-299. 7p.

Oral Medicine in Latin America and the Caribbean: A comprehensive survey of recognition, training, and practice.

Authors: Saldivia-Siracusa C González-Pérez LV Rivera C et al.

Source: Medicina oral, patologia oral y cirugia bucal [Med Oral Patol Oral Cir Bucal] 2025 May 01; Vol. 30 (3), pp. e363-e372. Date of Electronic Publication: 2025 May 01.

Publication Type: Journal Article; Observational Study

Journal Info: Publisher: Medicina Oral S.L Country of Publication: Spain NLM ID: 101231694 Publication Model: Electronic Cited Medium: Internet ISSN: 1698-6946 (Electronic) Linking ISSN: 16984447 NLM ISO Abbreviation: Med Oral Patol Oral Cir Bucal Subsets: MEDLINE

Expanding Phenotype of Poirier-Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients.

Authors: Orsini A Santangelo A Bravin F et al.

Source: Genes [Genes (Basel)] 2022 Jan 30; Vol. 13 (2). Date of Electronic Publication: 2022 Jan 30.

Publication Type: Journal Article

Journal Info: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE

Lacosamide effectiveness and tolerability in patients with drug-resistant epilepsy and severe disability under polytherapy: Therapy optimization as emerging from an observational study.

Authors: Pozzi M Zanotta N Epifanio R et al.

Source: Epilepsy & behavior : E&B [Epilepsy Behav] 2022 Mar; Vol. 128, pp. 108598. Date of Electronic Publication: 2022 Feb 09.

Publication Type: Journal Article; Observational Study; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Academic Press Country of Publication: United States NLM ID: 100892858 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-5069 (Electronic) Linking ISSN: 15255050 NLM ISO Abbreviation: Epilepsy Behav Subsets: MEDLINE

SCN2A Pathogenic Variants and Epilepsy: Heterogeneous Clinical, Genetic and Diagnostic Features.

Authors: Epifanio R Giorda R Merlano MC et al.

Source: Brain sciences [Brain Sci] 2021 Dec 24; Vol. 12 (1). Date of Electronic Publication: 2021 Dec 24.

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101598646 Publication Model: Electronic Cited Medium: Print ISSN: 2076-3425 (Print) Linking ISSN: 20763425 NLM ISO Abbreviation: Brain Sci Subsets: PubMed not MEDLINE

Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individuals.

Authors: Ricci E Fetta A Garavelli L et al.

Corporate Authors: Ricci E Fetta A Garavelli L et al.

Source: Epilepsy & behavior : E&B [Epilepsy Behav] 2021 Oct 04; Vol. 124, pp. 108315. Date of Electronic Publication: 2021 Oct 04.

Publication Type: Journal Article

Journal Info: Publisher: Academic Press Country of Publication: United States NLM ID: 100892858 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-5069 (Electronic) Linking ISSN: 15255050 NLM ISO Abbreviation: Epilepsy Behav Subsets: MEDLINE; PubMed not MEDLINE

Partial deletion of DEPDC5 in a child with focal epilepsy.

Authors: Bonaglia MC Giorda R Epifanio R et al.

Source: Epilepsia open [Epilepsia Open] 2016 Aug 25; Vol. 1 (3-4), pp. 140-144. Date of Electronic Publication: 2016 Aug 25 (Print Publication: 2016).

Publication Type: Journal Article

Journal Info: Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101692036 Publication Model: eCollection Cited Medium: Print ISSN: 2470-9239 (Print) Linking ISSN: 24709239 NLM ISO Abbreviation: Epilepsia Open Subsets: PubMed not MEDLINE

Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European study.

Authors: Raviglione F Douzgou S Scala M et al.

Source: Seizure [Seizure] 2021 May; Vol. 88, pp. 60-72. Date of Electronic Publication: 2021 Mar 30.

Publication Type: Journal Article; Multicenter Study

Journal Info: Publisher: Elsevier Country of Publication: England NLM ID: 9306979 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2688 (Electronic) Linking ISSN: 10591311 NLM ISO Abbreviation: Seizure Subsets: MEDLINE

Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype.

Authors: Cordelli DM Garavelli L Savasta S et al.

Source: American journal of medical genetics. Part A [Am J Med Genet A] 2013 Feb; Vol. 161A (2), pp. 273-84. Date of Electronic Publication: 2013 Jan 15.

Publication Type: Journal Article; Multicenter Study

Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature.

Authors: Vignoli A Borgatti R Peron A et al.

Source: Epilepsia [Epilepsia] 2012 Jul; Vol. 53 (7), pp. 1146-55. Date of Electronic Publication: 2012 May 11.

Publication Type: Case Reports; Journal Article; Review

Journal Info: Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE

Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.

Authors: Zucca C Redaelli F Epifanio R et al.

Source: Archives of neurology [Arch Neurol] 2008 Apr; Vol. 65 (4), pp. 489-94.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: American Medical Assn Country of Publication: United States NLM ID: 0372436 Publication Model: Print Cited Medium: Internet ISSN: 1538-3687 (Electronic) Linking ISSN: 00039942 NLM ISO Abbreviation: Arch Neurol Subsets: MEDLINE

Visual function in infants with West syndrome: correlation with EEG patterns.

Authors: Randò T Bancale A Baranello G et al.

Source: Epilepsia [Epilepsia] 2004 Jul; Vol. 45 (7), pp. 781-6.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print Cited Medium: Print ISSN: 0013-9580 (Print) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE

Novel epilepsy phenotype associated to a known SCN8A mutation.

Authors: Epifanio R Zanotta N Giorda R et al.

Source: Seizure [Seizure] 2019 Apr; Vol. 67, pp. 15-17. Date of Electronic Publication: 2019 Mar 04.

Publication Type: Case Reports; Letter

Journal Info: Publisher: Elsevier Country of Publication: England NLM ID: 9306979 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2688 (Electronic) Linking ISSN: 10591311 NLM ISO Abbreviation: Seizure Subsets: MEDLINE

Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.

Authors: Ivanovski I Djuric O Caraffi SG et al.

Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2018 Sep; Vol. 20 (9), pp. 965-975. Date of Electronic Publication: 2018 Jan 04.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Electrical status epilepticus during sleep in Mowat-Wilson syndrome.

Authors: Bonanni P Negrin S Volzone A et al.

Source: Brain & development [Brain Dev] 2017 Oct; Vol. 39 (9), pp. 727-734. Date of Electronic Publication: 2017 May 10.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 7909235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-7131 (Electronic) Linking ISSN: 03877604 NLM ISO Abbreviation: Brain Dev Subsets: MEDLINE

Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.

Authors: Garavelli L Ivanovski I Caraffi SG et al.

Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2017 Jun; Vol. 19 (6), pp. 691-700. Date of Electronic Publication: 2016 Nov 10.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE