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Biomechanical Multipurpose Miniscrew Strategy for Simultaneous Distalization in Class II Patients-The BiGa System

Biomimetics (Basel, Switzerland), 2024, Vol.9 (5)

2024

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Lower rates of readmission following integration of family-based treatment in a higher level of care

Eating Disorders, 2021, Vol.29 (6), p.677-684

2021

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Tibial fracture repair with angle-stable interlocking nailing in 2 calves

Veterinary surgery : VS, 2019, Vol.48 (4), p.597-606

2019

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Pseudohypoparathyroidism with Ectopic Calcification and 22q11 Deletion Syndrome: A Rare Case

Journal of pediatric genetics, 2021, Vol.10 (1), p.45-48

2021

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Multiloculated cerebral lesion in an immunocompromised patient heralding cerebral nocardiosis

Revue neurologique, 2020, Vol.176 (3), p.208-210

2020

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Unusual Characteristics and Variable Expressivity in a Brazilian Family with Cherubism

Journal of pediatric genetics, 2021, Vol.10 (1), p.63-69

2021

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Trisomy 21 and Ebstein Anomaly: Diagnosis and Prognosis of a Rare Association

Journal of pediatric genetics, 2021, Vol.10 (4), p.319-322

2021

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Locked-in syndrome following meningitis with brainstem abscess

Revue neurologique, 2019, Vol.175 (1-2), p.88-89

2019

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First Italian birth after cryopreserved ovarian tissue transplantation in a patient affected by non-Hodgkin's lymphoma

International journal of hematologic oncology, 2018, Vol.7 (4), p.IJH08-IJH08

2018

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The role of a femtosecond laser in congenital cataract associated with aniridia

Arquivos brasileiros de oftalmologia, 2018, Vol.81 (5), p.433-436

2018

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SARS-CoV-2-related ARDS in a maintenance hemodialysis patient: case report on tailored approach by daily hemodialysis, noninvasive ventilation, tocilizumab, anxiolytics, and point-of-care ultrasound

Clinical case reports, 2021, Vol.9 (2), p.694-703

2021

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Ophthalmologic Impairment and Intellectual Disability in a Girl Presenting Kenny-Caffey Syndrome Type 2

Journal of pediatric genetics, 2020, Vol.9 (4), p.263-269

2020

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Report of the Phenotype of a Patient with Roberts Syndrome and a Rare ESCO2 Variant

Journal of pediatric genetics, 2020, Vol.9 (1), p.58-62

2020

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WAGRO syndrome: a rare genetic condition associated with aniridia and additional ophthalmologic abnormalities

Arquivos brasileiros de oftalmologia, 2019, Vol.82 (4), p.336-338

2019

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TCRαβ CD19 depletion in allogeneic haematopoietic stem cell transplantation performed for Hurler syndrome

Bone marrow transplantation, 2016, Vol.51 (3), p.438-439

2016

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Clitoris cyst mimicking ambiguous genitalia and presenting spontaneous regression

Pediatrics international : official journal of the Japan Pediatric Society, 2019, Vol.61 (1), p.113-114

2019

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Chest Wall Resection for Single Rib Metastasis after Breast Cancer

The breast journal, 2015, Vol.21 (4), p.454-456

2015

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Is there an increased prevalence of Wilms' tumor in incontinentia pigmenti syndrome?

International journal of dermatology, 2014, Vol.53 (12), p.e578-e579

2014

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The role of inconstant perforating arteries in harvesting radial flaps

Plastic and reconstructive surgery, 2011, Vol.127 (1), p.484-485

2011

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Enteropathy-associated T cell lymphoma of the jejunum associated with colonic lymphocytosis with aberrant phenotype

Journal of clinical pathology, 2010, Vol.63 (9), p.850-852

2010

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Fat grafting according to Coleman for the treatment of radial nerve neuromas

Plastic and reconstructive surgery, 2010, Vol.126 (2), p.676-678

2010

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Nager syndrome and Pierre Robin sequence

Pediatrics International, 2015, Vol.57 (2), p.e69-e72

2015

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Haploidentical TCR A/B and B-cell depleted hematopoietic SCT in pediatric SAA and aspergillosis

Bone marrow transplantation, 2014, Vol.49 (6), p.847-849

2014

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Omphalocele-exstrophy-imperforate anus-spinal defects (OEIS) complex in a child with nail-patella syndrome

Pediatrics international : official journal of the Japan Pediatric Society, 2010, Vol.52 (5), p.847-848

2010

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Trisomy 12p syndrome secondary to a balanced familial translocation

Pediatrics International, 2010, Vol.52 (3), p.e144-e146

2010

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Biomechanical Multipurpose Miniscrew Strategy for Simultaneous Distalization in Class II Patients-The BiGa System

Lower rates of readmission following integration of family-based treatment in a higher level of care

Tibial fracture repair with angle-stable interlocking nailing in 2 calves

Pseudohypoparathyroidism with Ectopic Calcification and 22q11 Deletion Syndrome: A Rare Case

Multiloculated cerebral lesion in an immunocompromised patient heralding cerebral nocardiosis

Unusual Characteristics and Variable Expressivity in a Brazilian Family with Cherubism

Trisomy 21 and Ebstein Anomaly: Diagnosis and Prognosis of a Rare Association

Locked-in syndrome following meningitis with brainstem abscess

First Italian birth after cryopreserved ovarian tissue transplantation in a patient affected by non-Hodgkin's lymphoma

The role of a femtosecond laser in congenital cataract associated with aniridia

SARS-CoV-2-related ARDS in a maintenance hemodialysis patient: case report on tailored approach by daily hemodialysis, noninvasive ventilation, tocilizumab, anxiolytics, and point-of-care ultrasound

Ophthalmologic Impairment and Intellectual Disability in a Girl Presenting Kenny-Caffey Syndrome Type 2

Report of the Phenotype of a Patient with Roberts Syndrome and a Rare ESCO2 Variant

WAGRO syndrome: a rare genetic condition associated with aniridia and additional ophthalmologic abnormalities

TCRαβ CD19 depletion in allogeneic haematopoietic stem cell transplantation performed for Hurler syndrome

Clitoris cyst mimicking ambiguous genitalia and presenting spontaneous regression

Chest Wall Resection for Single Rib Metastasis after Breast Cancer

Is there an increased prevalence of Wilms' tumor in incontinentia pigmenti syndrome?

The role of inconstant perforating arteries in harvesting radial flaps

Enteropathy-associated T cell lymphoma of the jejunum associated with colonic lymphocytosis with aberrant phenotype

Fat grafting according to Coleman for the treatment of radial nerve neuromas

Nager syndrome and Pierre Robin sequence

Haploidentical TCR A/B and B-cell depleted hematopoietic SCT in pediatric SAA and aspergillosis

Omphalocele-exstrophy-imperforate anus-spinal defects (OEIS) complex in a child with nail-patella syndrome

Trisomy 12p syndrome secondary to a balanced familial translocation

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