• A case of recurrent gastrinoma in the liver with a review of "primary" hepatic gastrinomas
• A curable radicular syndrome in thoracolumbar spondylarthrosis
• A new hypothalamic syndrome; Intermittent oliguria with edema of the face and sexual disorders
• A special form of the syndrome of the superior orbital fissure
• Acute chest syndrome in sickle cell disease due to the new influenza A (H1N1) virus infection
• Addition of the nuclear export inhibitor selinexor to standard intensive treatment for elderly patients with acute myeloid leukemia and high risk myelodysplastic syndrome
• Alpha 1-antitrypsin deficiency and the flaccid lung syndrome. The heterozygote controversy
• Atrophy of the cerebellum with oculocutaneous and bronchial telangiectasis as a familial syndrome
• Azacitidine maintenance after intensive chemotherapy improves DFS in older AML patients
• Biemond syndrome
• Biemond's syndrome (a study of two cases)
• Biemond's syndrome in relatives with coloboma of the iris, coxofemoral dysplasia and epilepsy
• Cerebellar atrophy with oculocutaneous telangiectasis and bronchiectasis as a familial syndrome
• Chest pain in sickle cell disease
• Ciliopathy--cause of several peculiar syndromes
• Clinical-anatomical examination of a case of the so-called syndrome thalamique
• Coloboma, mental retardation, hypogonadism, and obesity: critical review of the so-called Biemond syndrome type 2, updated nosology, and delineation of three "new" syndromes
• Congenital cerebellar ataxia
• Continuous dexamethasone infusion for seven hours in patients with the Cushing syndrome. A superior differential diagnostic test
• Cooling the crisis: therapeutic hypothermia after sickle cardiac arrest
• Cortisol receptor resistance: the variability of its clinical presentation and response to treatment
• Determinants of lenalidomide response with or without erythropoiesis-stimulating agents in myelodysplastic syndromes: the HOVON89 trial
• Diagnostic efficacy of the secretin stimulation test for the Zollinger-Ellison syndrome: an intra-individual comparison using different dosages in patients and controls
• Diagnostic value of serum pepsinogen C in patients with raised serum concentrations of pepsinogen A
• Dynamics of von Willebrand factor reactivity in sickle cell disease during vaso-occlusive crisis and steady state
• Familial and iatrogenic cortisol receptor resistance
• Hereditary ataxia with sensory neuronopathy: Biemond's ataxia
• Hypothalamic syndromes in general and disturbances in the water regulation in particular
• Incentive spirometry to prevent acute chest syndrome in adults with sickle cell disease; a randomized controlled trial
• Inflammatory and endothelial markers during vaso-occlusive crisis and acute chest syndrome in sickle cell disease
• Lenalidomide added to standard intensive treatment for older patients with AML and high-risk MDS
• Lung Microbiota of Critically Ill Patients with COVID-19 Are Associated with Nonresolving Acute Respiratory Distress Syndrome
• Molecular characterization of mutant TP53 acute myeloid leukemia and high-risk myelodysplastic syndrome
• Nucleosomes and neutrophil activation in sickle cell disease painful crisis
• Occasional neurological syndrome with cerebral arteriosclerosis
• Ocular phenotypes of three genetic variants of Bardet-Biedl syndrome
• Patient-controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease, a randomized controlled trial
• Peptic ulcer, non-ulcer dyspepsia and irritable bowel syndrome in The Netherlands and Japan
• Platelet doubling after the first azacitidine cycle is a promising predictor for response in myelodysplastic syndromes (MDS), chronic myelomonocytic leukaemia (CMML) and acute myeloid leukaemia (AML) patients in the Dutch azacitidine compassionate named p
• Prospective evaluation of chronic organ damage in adult sickle cell patients: A seven-year follow-up study
• Proximal and distal gut hormone secretion in irritable bowel syndrome
• Second international round robin for the quantification of serum non-transferrin-bound iron and labile plasma iron in patients with iron-overload disorders
• Serum pepsinogens in patients with gastric diseases or after gastric surgery
• Sickle cell disease-related organ damage occurs irrespective of pain rate: implications for clinical practice
• Syndrome of polyneuropathy consecutive to the development of neoplastic formations, interesting the cranial and spinal roots (contribution to the study of the anatomoclinical forms of meningeal sarcomatosis)
• The continuous 7-hour intravenous dexamethasone suppression test in the differential diagnosis of ACTH-dependent Cushing's syndrome
• The flaccid lung syndrome and alpha 1-protease inhibitor deficiency
• The retinal ciliopathies
• The serological gastric biopsy: a non-endoscopical diagnostic approach in management of the dyspeptic patient: significance for primary care based on a survey of the literature
• The Use of an Errorless Learning Application to Support Re-Learning of (Instrumental) Activities for People Living with Korsakoff Syndrome
• Therapeutic value of clofarabine in younger and middle-aged (18-65 years) adults with newly diagnosed AML
• Tisagenlecleucel in Adult Relapsed or Refractory Diffuse Large B-Cell Lymphoma
• Vaso-occlusive crisis and acute chest syndrome in sickle cell disease due to 2019 novel coronavirus disease (COVID-19)
• Wernicke's encephalopathy and Korsakow's syndrome