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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

2213

PDF: 1177

HTML: 333
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

2235

PDF: 3029
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

1929

PDF: 1827
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

1924

PDF: 1636
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

3409

PDF: 1835

HTML: 449
Nutritional rickets in twins: a case report

D. Frasca, G. Morganti, S. Cherubini

30-06-2013

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

1297

PDF: 1182
Feeding of preterm infants and fortification of breast milk

Giovanna Mangili, Elena Garzoli

28-06-2017

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

9592

PDF: 5263

HTML: 964
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

2363

PDF: 5723
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

3387

PDF: 2249
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

15262

PDF: 7784

HTML: 1665
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

3370

PDF: 869

HTML: 421
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

2186

PDF: 1132

HTML: 633
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

2115

PDF: 1346
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

1433

PDF: 1306
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

1844

PDF: 1309

HTML: 364
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

1720

PDF: 525

HTML: 13
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

9618

PDF: 5569

HTML: 561

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Search Results

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

Nutritional rickets in twins: a case report

Feeding of preterm infants and fortification of breast milk

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

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

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

Turner-like Syndrome: a case report

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

Follow-up study of three cases of congenital microgastria

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

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