F. Mollica - Concepedia

Author

F. Mollica

Also Known As

F MOLLICA, F Mollica, F. MOLLICA, F. Mollica, FEDERICO MOLLICA, Federico Mollica, Federico Mòllica, MOLLICA, F, T. Papalia

135

Publications

994

Citations

H-Index

Concepts

All Affiliations

University of Catania Northwick Park Hospital University of Siena University of Bonn University of Naples Federico II

About

F. Mollica is an author at University of Catania specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	21	571
2	Public Health	4	4	79
3	Health Sciences	2	2	36
4	Natural Sciences	1	1	17
5	Allergy	1	1	153

F. Mollica

Publications

785

Citations

H-Index

Page 1

	Year	Citations
Effectiveness of early prednisone treatment in preventing the development of nephropathy in anaphylactoid purpura F. Mollica, Salvatore Livolti, R Garozzo, European Journal of Pediatrics GlomerulonephritisRenal FunctionAllergyLupus NephritisChronic Kidney Disease	1992	153
Hyporesponsiveness to intradermal administration of hepatitis B vaccine in insulin dependent diabetes mellitus S. Li Volti, Manuela Caruso‐Nicoletti, F Biazzo, Archives of Disease in Childhood Iddm V ControlsImmunodeficienciesHumoral ResponseImmunologyHepatitis B	1998	50
A case of cyclopia Role of environmental factors F. Mollica, G. Nuciforo, Giovanni Sorge Clinical Genetics Cyclopia RoleInfertilityVarious DrugsGynecologyReproductive Medicine	1979	34
A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosa M. G. S. Dunnill, Allan J. Richards, G. Mllana, Human Molecular Genetics Molecular Diagnostic TechniquesMendelian DisorderCollagen Vii GeneMedicineGenetics	1994	30
Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and Genotype BreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, Annals of the American Thoracic Society	2022	30
Schwartz-Jampel syndrome in two daughters of first cousins. Lorenzo Pavone, F. Mollica, Alexia Grasso, Journal of Neurology Neurosurgery & Psychiatry Developmental AnomalyRare Schwartz-jampel SyndromeSchwartz-jampel SyndromeGrowth Hormone SecretionGenetic Disorder	1978	29
Presentation of the data of the Italian registry for oculocutaneous tyrosinaemia A. Fois, P. Borgogni, M. Cioni, Journal of Inherited Metabolic Disease	1986	29
Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities. M. G. S. Dunnill, Allan J. Richards, Gabriella Milana, Journal of Medical Genetics GeneticsFibril AbnormalitiesLinkage AnalysisPathologyGenetic Linkage	1994	28
Asymptomatic type II hyperprolinaemia associated with hyperglycinaemia in three sibs. F. Mollica, Harvey L. Levy Archives of Disease in Childhood Metabolic SyndromeAutoimmune DiseaseMetabolic DisorderNeurological DisorderMedicine	1975	24
A prospective study of 18 infants of chronic HBsAg mothers. F. Mollica, S Musumeli, Sousa Suppo Rugolo, Archives of Disease in Childhood ImmunologyFetal MedicineMaternal ImmunizationHbsag CarriersPregnant Sicilian Women	1979	23

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