Published in Presse Med on March 22, 1967
Ophthalmic manifestations of the battered-baby syndrome. Br Med J (1971) 1.05
Ocular damage in the battered-baby syndrome. Br Med J (1971) 1.01
A 12-year ophthalmologic experience with the shaken baby syndrome at a regional children's hospital. Trans Am Ophthalmol Soc (1999) 0.98
The American-European Consensus Conference on ARDS. Definitions, mechanisms, relevant outcomes, and clinical trial coordination. Am J Respir Crit Care Med (1994) 27.68
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. Nature (1994) 4.04
Metabolic and respiratory changes after cholecystectomy performed via laparotomy or laparoscopy. Br J Anaesth (1992) 3.50
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Cytokine serum level during severe sepsis in human IL-6 as a marker of severity. Ann Surg (1992) 2.96
[Thanatophoric dwarfism]. Presse Med (1967) 2.25
Antithrombin III in patients with severe sepsis. A randomized, placebo-controlled, double-blind multicenter trial plus a meta-analysis on all randomized, placebo-controlled, double-blind trials with antithrombin III in severe sepsis. Intensive Care Med (1998) 2.12
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A gene for hereditary multiple exostoses maps to chromosome 19p. Hum Mol Genet (1994) 2.00
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy. Cell (1995) 1.95
Pain after laparoscopic cholecystectomy: characteristics and effect of intraperitoneal bupivacaine. Anesth Analg (1995) 1.92
Tumor necrosis factor and interleukin-1 serum levels during severe sepsis in humans. Crit Care Med (1989) 1.83
Cortical processing of noxious somatosensory stimuli in the persistent vegetative state. Neuroimage (2002) 1.71
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Acquired immunodeficiency syndrome in African patients. N Engl J Med (1984) 1.70
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Restoration of thalamocortical connectivity after recovery from persistent vegetative state. Lancet (2000) 1.59
Pathogenic mechanisms in osteochondrodysplasias. J Bone Joint Surg Am (1984) 1.58
Parental consanguinity in two sibs with omodysplasia. Am J Med Genet (1994) 1.56
Incomplete penetrance and expressivity skewing in hereditary multiple exostoses. Clin Genet (1997) 1.49
Postoperative spirometry after laparoscopy for lower abdominal or upper abdominal surgical procedures. Br J Anaesth (1997) 1.48
Epstein-Barr virus serology and Epstein-Barr virus-associated lymphoproliferative disorders in pediatric liver transplant recipients. Transplantation (1993) 1.47
[5 cases of microgeodic disease of phalanges of unknown etiology in infants]. Ann Radiol (Paris) (1970) 1.47
Occupational stress and burnout in anaesthesia. Br J Anaesth (2003) 1.46
Guidelines for the transfusion of red cells. Acta Clin Belg (2009) 1.41
Euthanasia: a law in Belgium? Intensive Care Med (2001) 1.38
Laryngeal mask. Intensive Care World (1993) 1.37
Neural mechanisms of antinociceptive effects of hypnosis. Anesthesiology (2000) 1.32
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Use of the neodymium-YAG laser to open the posterior capsule after lens implant surgery: a preliminary report. J Am Intraocul Implant Soc (1980) 1.32
Acromicric dysplasia. Am J Med Genet (1986) 1.28
Auditory processing in the vegetative state. Brain (2000) 1.28
The lethal osteochondrodysplasias. Adv Hum Genet (1990) 1.28
An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature. Hum Genet (1990) 1.28
Stop codon FGFR3 mutations in thanatophoric dwarfism type 1. Nat Genet (1995) 1.27
[Metachondromatosis]. Z Kinderheilkd (1971) 1.26
Cerebral tumors in infancy. 66 clinicoanatomical case studies. Am J Dis Child (1968) 1.26
Multiple epiphyseal dysplasia, Fairbank type: morphologic and biochemical study of cartilage. Am J Med Genet (1993) 1.22
[Generalized hyperostosis corticalis (dominant transmission) (Worth's type)]. Arch Fr Pediatr (1972) 1.22
Diagnostic and prognostic use of bispectral index in coma, vegetative state and related disorders. Brain Inj (2008) 1.21
[Metatrophic dwarfism]. Arch Kinderheilkd (1966) 1.21
[Ophthalmological use of pulsated Neodymium Yag lasers. Preoperative aperture of lenses previous setting in of artificial lenses and opening of secondary cataracts behind implants (author's transl)]. J Fr Ophtalmol (1981) 1.21
[The campomelic syndrome]. Presse Med (1971) 1.21
Opsismodysplasia: a new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebrae. Am J Med Genet (1984) 1.18
Clinical, radiological, and chondro-osseous findings in opsismodysplasia: survey of a series of 12 unreported cases. J Med Genet (2003) 1.16
Common mutations in the fibroblast growth factor receptor 3 (FGFR 3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfism. Am J Med Genet (1996) 1.14
[Lethal osteogenesis imperfecta. Definition and heterogeneity]. Ann Genet (1984) 1.14
Operative mortality following surgery for colorectal cancer. Br J Surg (1989) 1.13
The Dyggve-Melchior-Clausen syndrome. Radiology (1975) 1.13
Proteoglycan populations of baboon (Papio papio) articular cartilage. Biochem J (1977) 1.12
Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome. Hum Genet (1988) 1.11
The biochemical defect of pseudoachondroplasia. Eur J Pediatr (1982) 1.10
Oligosaccharidoses. A new concept. Arch Fr Pediatr (1977) 1.09
Clonidine and ketanserin both are effective treatment for postanesthetic shivering. Anesthesiology (1993) 1.09
Fragilitas ossium: a new autosomal recessive mutation in the mouse. J Hered (1982) 1.08
Structure of nine sialyl-oligosaccharides accumulated in urine of eleven patients with three different types of sialidosis. Mucolipidosis II and two new types of mucolipidosis. Eur J Biochem (1977) 1.08
Gel electrophoretic studies on proteoglycans and collagen of abnormal human growth cartilage: proteoglycan abnormalities in pseudoachondroplasia and in Kniest's disease. Pediatr Res (1975) 1.07
[Fibrochondrogenesis]. Arch Fr Pediatr (1978) 1.06
IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies. J Clin Endocrinol Metab (1999) 1.05
Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2. Am J Med Genet (1998) 1.05
Effects of training on exercise-induced muscle damage and interleukin 6 production. Muscle Nerve (1999) 1.05
Mild endotoxaemia and the inflammatory response induced by a marathon race. Clin Sci (Lond) (1997) 1.04
Are similar inflammatory factors involved in strenuous exercise and sepsis? Intensive Care Med (1994) 1.04
Atelosteogenesis. Am J Med Genet (1982) 1.04
Pathologic features and mechanisms of hypoxemia in adult respiratory distress syndrome. Am Rev Respir Dis (1976) 1.03
Achondrogenesis within the scope of connately manifested generalized skeletal dysplasias. Z Kinderheilkd (1974) 1.02
Achondroplasia in man and animals. Clin Orthop Relat Res (1968) 1.01
Psychological approaches during conscious sedation. Hypnosis versus stress reducing strategies: a prospective randomized study. Pain (1997) 1.00
Revisiting metatropic dysplasia: presentation of a series of 19 novel patients and review of the literature. Am J Med Genet A (2008) 1.00
Mazabraud syndrome in two patients: clinical overlap with McCune-Albright syndrome. Am J Med Genet (2001) 1.00
[Fibroblasts in culture during mucopolysaccharidoses: the effect of serum on metachromasy]. Ann Genet (1968) 1.00
[The genetics of congenital glaucoma: a study of 231 cases]. J Genet Hum (1976) 1.00
Desbuquois syndrome. Eur J Pediatr (1991) 1.00
Incontinentia pigmenti (IP) and r(X). Tentative mapping of the IP locus to the X juxtacentromeric region. Ann Genet (1985) 1.00
Functional neuroanatomy of hypnotic state. Biol Psychiatry (1999) 0.99
Morphological and biochemical studies of a mouse mutant (fro/fro) with bone fragility. Bone (1991) 0.99
Cytotoxicity towards human endothelial cells, induced by neutrophil myeloperoxidase: protection by ceftazidime. Mediators Inflamm (1995) 0.99
Pulmonary pathology in acute respiratory insufficiency: lung biopsy as a diagnostic tool. J Thorac Cardiovasc Surg (1976) 0.99
[Diagnosis of chondrodystrophic dwarfism in the newborn]. Arch Fr Pediatr (1968) 0.98
Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3. J Med Genet (2003) 0.98
[Acromesomelic dwarfism]. Presse Med (1971) 0.97
[Hurler's pseudo-polydystrophy]. Presse Med (1966) 0.97
New approaches and old controversies to postoperative pain control following cardiac surgery. Eur J Anaesthesiol (2006) 0.97
Langer-Giedion syndrome with and without del 8q. assignment of critical segment to 8q23. Hum Genet (1982) 0.97
Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasia. J Med Genet (1996) 0.97
Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance. J Med Genet (2001) 0.96
Toulouse-Lautrec's diagnosis. Nat Genet (1995) 0.96
[Acrodysostosis]. Presse Med (1968) 0.96
Myocellular enzyme leakage, polymorphonuclear neutrophil activation and delayed onset muscle soreness induced by isokinetic eccentric exercise. Arch Physiol Biochem (1996) 0.96
Functional MRI of sustained attention in bipolar mania. Mol Psychiatry (2010) 0.96
[Poland's syndrome. Clinical and genetic studies; physiopathologic considerations]. Nouv Presse Med (1976) 0.96
Red blood cell substitutes: fluorocarbon emulsions and haemoglobin solutions. Br Med Bull (1999) 0.95
Epidural anesthesia impairs both central and peripheral thermoregulatory control during general anesthesia. Anesthesiology (1994) 0.95
Clinical and genetic heterogeneity of hypochondroplasia. J Med Genet (1996) 0.95
Mutations of the fibroblast growth factor receptor-3 gene in achondroplasia. Horm Res (1996) 0.95