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Kearns-Sayre syndrome with facial and white matter extensive involvement: a (mitochondrial and nuclear gene related?) neurocristopathy?

Agostino Berio, Attilia Piazzi, Carlo Enrico Traverso

15-12-2017

https://doi.org/10.4081/pmc.2017.169

2273

Downloads: 1232

HTML: 337
Hyperammonemic coma in a patient with late-onset OTC deficiency

V. Dâ€™Onofrio, F. Poma, A. Enea, F. Santarelli, C. Lovera, M. Spada

30-06-2014

https://doi.org/10.4081/pmc.2014.9

2289

Downloads: 3074
Multiple endocrinopathies (growth hormone deficiency, autoimmune hypothyroidism and diabetes mellitus) in Kearns-Sayre syndrome

A. Berio, A. Piazzi

30-06-2013

https://doi.org/10.4081/pmc.2013.48

2016

Downloads: 1912
Cross-sectional and prospective study of the effects of GH therapy on metabolic panel in children with GH deficiency

V. Ramistella, M. Wasniewska, S. Arasi, M. Catena, M.R. Velletri, D. Corica, S. Santucci, F. De Luca

30-12-2014

https://doi.org/10.4081/pmc.2014.104

1968

Downloads: 1693
Nutritional problems of children with bronchopulmonary dysplasia after hospital discharge

Gianluca Lista, Fabio Meneghin, Ilia Bresesti, Francesco Cavigioli

22-12-2017

https://doi.org/10.4081/pmc.2017.183

3456

Downloads: 1887

HTML: 457
Feeding of preterm infants and fortification of breast milk

Giovanna Mangili, Elena Garzoli

28-06-2017

https://doi.org/10.4081/pmc.2017.158

9668

Downloads: 5332

HTML: 968
Nutritional rickets in twins: a case report

D. Frasca, G. Morganti, S. Cherubini

30-06-2013

https://doi.org/10.4081/pmc.2013.46

1333

Downloads: 1228
A not very essential obesity: the Rohhad Syndrome. Description of two cases and review of the literature

V. Ramistella, M. Wasniewska, M. Valenzise, D. Corica, S. Cantucci, E. Pitrolo, M. Romeo, F. De Luca

31-08-2013

https://doi.org/10.4081/pmc.2013.40

2405

Downloads: 5765
Generalized aggressive periodontitis in prepubertal age: description and comparison of two cases

G. Piergallini, A. Malerba, L. Mazzucchelli, L. Strohmenger

31-08-2014

https://doi.org/10.4081/pmc.2014.95

3436

Downloads: 2280
Nutritional and metabolic programming during the first thousand days of life

Massimo Agosti, Francesco Tandoi, Laura Morlacchi, Angela Bossi

28-06-2017

https://doi.org/10.4081/pmc.2017.157

15395

Downloads: 7942

HTML: 1675
Challenges in diagnosis and treatment of Cushing disease in a 12-year-old boy

Agim Gjikopulli, Sonila Tomori, Marjeta Tanka, Donjeta Bali

11-02-2025

https://doi.org/10.4081/pmc.2025.340

3450

Downloads: 926

HTML: 438
Turner-like Syndrome: a case report

M.R. Velletri, M. Valenzise, M. Wasniewska, S. Arasi, A. Santisi, M. Romeo, E. Pitrolo, S. Santucci, D. Corica, R. Crisafulli, G. Zirilli

31-10-2013

https://doi.org/10.4081/pmc.2013.33

1467

Downloads: 1329
Utility of a stool antigen test to detect the incidence of helicobacter pylori infection and familial and community enviromental risk factors for this infection in pediatric age

T. Sabbi, L. Dallâ€™Oglio, P. De Angelis, F. Torroni, F. Colistro, M. Azzolina, A. Santoni, V. Di Ciommo, M. Benedetto

30-04-2012

https://doi.org/10.4081/pmc.2012.66

2191

Downloads: 1447
Oculo-auriculo-vertebral spectrum with craniosynostosis and osteo-cartilagineous multiple defects: a diffuse chondro-membranous-osteo-dysplasia

Agostino Berio, Giacomo Garlaschi, Giuseppe Mangiante, Attilia Piazzi

29-12-2015

https://doi.org/10.4081/pmc.2015.123

2235

Downloads: 1181

HTML: 635
Weaning and complementary feeding in preterm infants: management, timing and health outcome

Roberta Barachetti, Elisabetta Villa, Mario Barbarini

22-12-2017

https://doi.org/10.4081/pmc.2017.181

9691

Downloads: 5641

HTML: 566
Follow-up study of three cases of congenital microgastria

Sara Ugolini, Chiara Oreglio, Karl Christian Walsh, Antonino Morabito

15-12-2023

https://doi.org/10.4081/pmc.2023.326

2149

Downloads: 602

HTML: 16
Oculo-auriculo-vertebral spectrum with myopathy and velopharyngeal insufficiency. A case report with a non-branchiomeric muscle biopsy

Giovanni Murialdo, Attilia Piazzi, Giuseppe Badolati, Enrico Calcagno, Agostino Berio

27-06-2016

https://doi.org/10.4081/pmc.2016.121

1882

Downloads: 1362

HTML: 364

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Kearns-Sayre syndrome with facial and white matter extensive involvement: a (mitochondrial and nuclear gene related?) neurocristopathy?

Hyperammonemic coma in a patient with late-onset OTC deficiency

Multiple endocrinopathies (growth hormone deficiency, autoimmune hypothyroidism and diabetes mellitus) in Kearns-Sayre syndrome

Cross-sectional and prospective study of the effects of GH therapy on metabolic panel in children with GH deficiency

Nutritional problems of children with bronchopulmonary dysplasia after hospital discharge

Feeding of preterm infants and fortification of breast milk

Nutritional rickets in twins: a case report

A not very essential obesity: the Rohhad Syndrome. Description of two cases and review of the literature

Generalized aggressive periodontitis in prepubertal age: description and comparison of two cases

Nutritional and metabolic programming during the first thousand days of life

Challenges in diagnosis and treatment of Cushing disease in a 12-year-old boy

Turner-like Syndrome: a case report

Utility of a stool antigen test to detect the incidence of helicobacter pylori infection and familial and community enviromental risk factors for this infection in pediatric age

Oculo-auriculo-vertebral spectrum with craniosynostosis and osteo-cartilagineous multiple defects: a diffuse chondro-membranous-osteo-dysplasia

Weaning and complementary feeding in preterm infants: management, timing and health outcome

Follow-up study of three cases of congenital microgastria

Oculo-auriculo-vertebral spectrum with myopathy and velopharyngeal insufficiency. A case report with a non-branchiomeric muscle biopsy

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