[Wiedemann-Beckwith syndrome. Clinical and metabolic study of 4 cases]

["NPAs": a new allergic risk?].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2009

[The history of tuberculosis].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2005

Comparison of the efficacy and safety of nebulized beclometasone dipropionate and budesonide in severe persistent childhood asthma.

Respiratory medicine·2003

[Asthma and food allergy: report of 163 pediatric cases].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2002

[Asthma in infants and young children: definitions and epidemiology].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2002

[Lung abscess due to Mycoplasma pneumoniae in an adolescent].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2002

[Psychological aspects of bone marrow donation in donor brothers and sisters in bone marrow transplantation].

Pediatrie·1993

[Lethargy in the course of treatment with ranitidine in a newborn infant].

Pediatrie·1993

[Delayed detection of hip dislocation: is the physician to blame?].

Pediatrie·1993

[Renal tubular acidosis in children].

Pediatrie·1993

[CD23: structures, functions and practical perspectives in allergy reactions].

Pediatrie·1993

[Accessory thymus in cervical ectopy: apropos of a case].

Pediatrie·1993

Guillain-Barré Syndrome.

Continuum (Minneapolis, Minn.)·2026

Clinical characteristics, genotype-phenotype correlation, and prognostic follow-up of 48 Chinese children with hereditary spherocytosis.

Frontiers in medicine·2026

Towards sustainable multidisciplinary renal cancer tumour boards: redesigning the referral pathway.

BJU international·2026

Clinical and Ultrasound Characteristics of High-Grade Endometrial Stromal Sarcoma.

Journal of clinical ultrasound : JCU·2026

Comorbidities increase the severity of COVID-19: an analysis and epidemiological study conducted in Algeria.

The Libyan journal of medicine·2026

A rare case of hereditary spastic paraplegia with homozygous mutation in the ZFYVE26 gene.

Ideggyogyaszati szemle·2026

Related Experiment Videos

[Wiedemann-Beckwith syndrome. Clinical and metabolic study of 4 cases]

Related Concept Videos

["NPAs": a new allergic risk?].

[The history of tuberculosis].

Comparison of the efficacy and safety of nebulized beclometasone dipropionate and budesonide in severe persistent childhood asthma.

[Asthma and food allergy: report of 163 pediatric cases].

[Asthma in infants and young children: definitions and epidemiology].

[Lung abscess due to Mycoplasma pneumoniae in an adolescent].

[Psychological aspects of bone marrow donation in donor brothers and sisters in bone marrow transplantation].

[Lethargy in the course of treatment with ranitidine in a newborn infant].

[Delayed detection of hip dislocation: is the physician to blame?].

[Renal tubular acidosis in children].

[CD23: structures, functions and practical perspectives in allergy reactions].

[Accessory thymus in cervical ectopy: apropos of a case].

Guillain-Barré Syndrome.

Clinical characteristics, genotype-phenotype correlation, and prognostic follow-up of 48 Chinese children with hereditary spherocytosis.

Towards sustainable multidisciplinary renal cancer tumour boards: redesigning the referral pathway.

Clinical and Ultrasound Characteristics of High-Grade Endometrial Stromal Sarcoma.

Comorbidities increase the severity of COVID-19: an analysis and epidemiological study conducted in Algeria.

A rare case of hereditary spastic paraplegia with homozygous mutation in the ZFYVE26 gene.

Related Experiment Videos

[Wiedemann-Beckwith syndrome. Clinical and metabolic study of 4 cases]

Related Concept Videos

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