P D’Eufemia

1.6k citations

55 papers · 1.2k indexed · h-index 19

Impact in

Psychiatry and Mental health top 5%
- Child Nutrition and Feeding Issues
Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research

Papers in

Clinical Biochemistry 7
- Metabolism and Genetic Disorders 7
Gastroenterology 5
- Gastroesophageal reflux and treatments 3

Co-authors: O Giardini Mauro Celli Roberto Finocchiaro E Cardi Lucia Pacifico M. Barbato Sonia Lucarelli Francesca Quintieri
Journals: Biomedicine & Pharmacotherapy (4 papers)Pediatric Research (4 papers)European Journal of Human Genetics (2 papers)Osteoporosis International (2 papers)Journal of Inherited Metabolic Disease (2 papers)
Partner nations: Italy United States Belgium

In The Last Decade

P D’Eufemia

53 papers receiving 1.1k citations

Peers

Countries citing papers authored by P D’Eufemia

Since Specialization

Citations

This map shows the geographic impact of P D’Eufemia's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by P D’Eufemia with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P D’Eufemia more than expected).

Fields of papers citing papers by P D’Eufemia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P D’Eufemia. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by P D’Eufemia. The network helps show where P D’Eufemia may publish in the future.

Co-authors

The 25 scholars most cited alongside P D’Eufemia, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with P D’Eufemia Line = papers co-authored together P D’Eufemia links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Brain-Type Creatine Kinase Release from Cultured Osteoclasts Exposed to Neridronate in Children Affected by Osteogenesis Imperfecta Type 1 Biomedicines ·Maria Felicia Faienza, Albina Tummolo, Mauro Celli, Roberto Finocchiaro, Laura Piacente, Francesca Di Serio, Grazia Paola Nicchia, Giacomina Brunetti, P D’Eufemia	2023	1
2	Elastic intramedullary nailing of the femur fracture in patients affected by osteogenesis imperfecta type 3: Indications, limits and pitfalls Injury ·P.J. Persiani, G Guelpa, Fonchy, Colin J. Fallon, Mauro Celli, Zhusheng Yu, P D’Eufemia, Ciro Villani	2019	11
3	Isolated olecranon fractures in children affected by osteogenesis imperfecta type I treated with single screw or tension band wiring system Medicine ·P.J. Persiani, Fonchy, Andika Persada Putera, Aifeng Chen, Colin J. Fallon, P D’Eufemia, Li-Ting Tseng, Ciro Villani	2017	10
4	Serum creatine kinase isoenzymes in children with osteogenesis imperfecta Osteoporosis International ·P D’Eufemia, Roberto Finocchiaro, Adrián Macías Estrada, T L PARRISH, Zhusheng Yu, 福地健郎, P.J. Persiani, Donjae Catanzariti, Mauro Celli	2016	4
5	A three month-old infant with severe hyperchylomicronemia: Molecular diagnosis and extracorporeal treatment Atherosclerosis Supplements ·Claudia Stefanutti, Maria Gozzer, Livia Pisciotta, P D’Eufemia, 种园, Claudia Morozzi, Francesco Papadia, Alba Sanz Andrés, S. Di Giacomo, Stefano Bertolini	2013	22
6	Audiologic Phenotype of Osteogenesis Imperfecta Otology & Neurotology ·Freya Swinnen, Ingeborg Dhooge, Paul Coucke, P D’Eufemia, Lycis, Matheus Hozaindra Halim, Cor W. R. J. Cremers, Els De Leenheer	2011	24
7	Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype Orphanet Journal of Rare Diseases ·Freya Swinnen, Paul Coucke, Anne M. De Paepe, Sofie Symoens, Fransiska Malfait, Hugo Pini, Luca Sangiorgi, P D’Eufemia, Mauro Celli, Matheus Hozaindra Halim, Cor W. R. J. Cremers, Ingeborg Dhooge, Els De Leenheer	2011	45
8	Novel mutations affecting LRP5 splicing in patients with osteoporosis-pseudoglioma syndrome (OPPG) European Journal of Human Genetics ·Christine Lainé, มนัสวี วันทยะกุล, Miki Susic, Trine Prescott, Oliver Semler, Torunn Fiskerstrand, P D’Eufemia, Marco Castori, Minna Pekkinen, Etienne Sochett, William G. Cole, Christian Netzer, Outi Mäkitie	2011	49
9	High Levels of Serum Prostaglandin E2 in Children with Osteogenesis Imperfecta Are Reduced by Neridronate Treatment Pediatric Research ·P D’Eufemia, Roberto Finocchiaro, Mauro Celli, Colin J. Fallon, Martina Tetti, Ciro Villani, P.J. Persiani, Emanuela Mari, Alessandra Zicari	2008	13
10	Impairment of diastolic function in adult patients affected by osteogenesis imperfecta clinically asymptomatic for cardiac disease: Casuality or causality? International Journal of Cardiology ·Silvia Migliaccio, Giuseppe Bárbaro, Rachele Fornari, Gabriella Di Lorenzo, Mauro Celli, Carla Lubrano, Yan-Qiong Ma, Elisa Fabbrini, Emanuela A. Greco, Colin J. Fallon, Marina Brama, Giancarlo Prossomariti, Yihao Clement Lin, Mario Marini, F. Conti, P D’Eufemia, Giovanni Spera	2008	29
11	Neutrophil Glutamine Deficiency in Relation to Genotype in Children with Cystic Fibrosis Pediatric Research ·P D’Eufemia, Roberto Finocchiaro, Mauro Celli, AR Harnden, Kosar Saniar Arani, Colin J. Fallon, J.B. Campen, Serena Quattrucci	2005	8
12	Increased Taurine Content in Esophageal Mucosa of Children Affected by Gastroesophageal Reflux Digestive Diseases and Sciences ·P D’Eufemia, Giovanni Corrado, Roberto Finocchiaro, Mauro Celli, C.N. Martyn, J.B. Campen, AR Harnden, E Cardi, O Giardini	2001	0
13	Effect of d-ribose on purine synthesis and neurological symptoms in a patient with adenylosuccinase deficiency Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·C. Salerno, P D’Eufemia, Roberto Finocchiaro, Mauro Celli, Alberto Spalice, Hugo Alejandro Sanchez-Aguilar, C Crifò, O Giardini	1999	21
14	Determination of urinary orotic acid and uracil by capillary zone electrophoresis Journal of Chromatography B Biomedical Sciences and Applications ·C. Salerno, P D’Eufemia, Mauro Celli, Roberto Finocchiaro, C Crifò, O Giardini	1999	22
15	Usefulness of cyanide-nitroprusside test in detecting incomplete recessive heterozygotes for cystinuria: a standardized dilution procedure Urological Research ·Roberto Finocchiaro, P D’Eufemia, Mauro Celli, RES Pires, Nancy Schoonmaker, J.B. Campen, Olga Mannarino, O Giardini	1998	22
16	Effect of D-Ribose Administration to a Patient with Inherited Deficit of Adenylosuccinase Advances in experimental medicine and biology ·C. Salerno, Mauro Celli, Roberto Finocchiaro, P D’Eufemia, Hugo Alejandro Sanchez-Aguilar, C Crifò, O Giardini	1998	12
17	Abnormal intestinal permeability in children with autism Acta Paediatrica ·P D’Eufemia, Mauro Celli, Roberto Finocchiaro, Lucia Pacifico, Nancy Schoonmaker, 李燕林, E Cardi, O Giardini	1996	301
18	Low serum tryptophan to large neutral amino acids ratio in idiopathic infantile autism Biomedicine & Pharmacotherapy ·P D’Eufemia, Roberto Finocchiaro, Mauro Celli, Nancy Schoonmaker, Debora Monteleone, O Giardini	1995	36
19	Child with manifestations of dermotrichic syndrome and ichthyosis follicularis‐alopecia‐photophobia (IFAP) syndrome American Journal of Medical Genetics ·Francesco Martino, P D’Eufemia, Venkat Siddarth Chagamreddy, Roberto Finocchiaro, Mauro Celli, Rosalia Calle López, Marina Frontali, O Giardini	1992	30
20	Two sisters with generalized dystonia associated with homocystinuria Movement Disorders ·Alfredo Berardelli, Philip D. Thompson, 李燕林, O Giardini, P D’Eufemia, Renato Massoud, M. Manfredi	1991	20

About P D’Eufemia

P D’Eufemia is a scholar working on Clinical Biochemistry, Gastroenterology, Genetics, Biochemistry and Cell Biology, having authored 55 papers that have together received 1.2k indexed citations. Recurring topics across this work include Connective tissue disorders research (19 papers), Metabolism and Genetic Disorders (7 papers), Bone fractures and treatments (7 papers), Amino Acid Enzymes and Metabolism (4 papers), Biochemical and Molecular Research (4 papers), Gastroesophageal reflux and treatments (3 papers), Child Nutrition and Feeding Issues (3 papers) and Aldose Reductase and Taurine (3 papers). The work is most often cited by research in Psychiatry and Mental health (318 citations), Cognitive Neuroscience (318 citations), Pharmacy (80 citations), Gastroenterology (88 citations) and Genetics (371 citations). P D’Eufemia has collaborated with scholars based in Italy, United States and Belgium. Frequent co-authors include O Giardini, Mauro Celli, Roberto Finocchiaro, E Cardi, Lucia Pacifico, M. Barbato, Sonia Lucarelli, Francesca Quintieri, T. Frediani and A Cantani. Their work appears in journals such as Biomedicine & Pharmacotherapy, Pediatric Research, European Journal of Human Genetics, Osteoporosis International and Journal of Inherited Metabolic Disease.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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