[Morquio's syndrome--mucopolysaccharidosis type IV (clinical-genealogic study)]

[Improving renal cancer care].

Urologiia (Moscow, Russia : 1999)·2018

A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.

Endocrine journal·1999

[Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes].

Genetika·1996

[Treatment of closed fractures in children].

Khirurgiia·1995

[Congenital and acquired deformities of knee joint menisci in children].

Khirurgiia·1994

A single base mutation in the type II procollagen gene (COL2A1) that converts glycine alpha 1-247 to serine in a family with late-onset spondyloepiphyseal dysplasia.

Human mutation·1994

[Atlanto-axial instability in injuries of the ligament system in children and adolescents].

Ortopediia travmatologiia i protezirovanie·1991

[Roentgenological diagnosis of dystrophic bone cysts in children].

Ortopediia travmatologiia i protezirovanie·1991

[Computerized tomography in the diagnosis and control of the effectiveness of the treatment of injuries of the Achilles tendon].

Ortopediia travmatologiia i protezirovanie·1991

[Surgical treatment of scoliosis by the Armstrong method].

Ortopediia travmatologiia i protezirovanie·1991

[Injuries of the spine and spinal cord associated with other injuries].

Ortopediia travmatologiia i protezirovanie·1991

[Supratrochanteric osteotomy of the hip in adults with dysplastic coxarthrosis].

Ortopediia travmatologiia i protezirovanie·1991

Narrow Band Imaging Improves Endoscopic Differentiation of Inverted Papillomas From Nasal Polyps.

The Laryngoscope·2026

Epidemiological, Clinical and Viral Genomic Features of Influenza Virus Infections Among Pilgrims During the Grand Magal of Touba Over 7 Years (2018-2024).

Journal of medical virology·2026

Delayed Diagnosis of Common Variable Immunodeficiency Revealed by Recurrent Respiratory Infections and Persistent Mediastinal Lymphadenopathy: A Case Report.

Cureus·2026

Association Between UGT1A9 rs13418420 Polymorphism and Propofol Induction Characteristics in Chinese Female Patients Undergoing Brief Gynecological Procedures.

Pharmacogenomics and personalized medicine·2026

Clinical pearls and pitfalls in inborn errors of immunity: An expert-derived framework for diagnostic pattern recognition.

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology·2026

Inebilizumab in AQP4-Seropositive NMOSD: One-Year Follow-Up From a Multicenter, Real-World Study.

Annals of clinical and translational neurology·2026

Related Experiment Videos

[Morquio's syndrome--mucopolysaccharidosis type IV (clinical-genealogic study)]

Related Concept Videos

[Improving renal cancer care].

A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.

[Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes].

[Treatment of closed fractures in children].

[Congenital and acquired deformities of knee joint menisci in children].

A single base mutation in the type II procollagen gene (COL2A1) that converts glycine alpha 1-247 to serine in a family with late-onset spondyloepiphyseal dysplasia.

[Atlanto-axial instability in injuries of the ligament system in children and adolescents].

[Roentgenological diagnosis of dystrophic bone cysts in children].

[Computerized tomography in the diagnosis and control of the effectiveness of the treatment of injuries of the Achilles tendon].

[Surgical treatment of scoliosis by the Armstrong method].

[Injuries of the spine and spinal cord associated with other injuries].

[Supratrochanteric osteotomy of the hip in adults with dysplastic coxarthrosis].

Narrow Band Imaging Improves Endoscopic Differentiation of Inverted Papillomas From Nasal Polyps.

Epidemiological, Clinical and Viral Genomic Features of Influenza Virus Infections Among Pilgrims During the Grand Magal of Touba Over 7 Years (2018-2024).

Delayed Diagnosis of Common Variable Immunodeficiency Revealed by Recurrent Respiratory Infections and Persistent Mediastinal Lymphadenopathy: A Case Report.

Association Between UGT1A9 rs13418420 Polymorphism and Propofol Induction Characteristics in Chinese Female Patients Undergoing Brief Gynecological Procedures.

Clinical pearls and pitfalls in inborn errors of immunity: An expert-derived framework for diagnostic pattern recognition.

Inebilizumab in AQP4-Seropositive NMOSD: One-Year Follow-Up From a Multicenter, Real-World Study.

Related Experiment Videos

[Morquio's syndrome--mucopolysaccharidosis type IV (clinical-genealogic study)]

Related Concept Videos

Related Articles