Disease: Christian syndrome
- 2 clinical cases of an osseous form of chronic xanthomatosis (Hand-Schueller-Christian syndrome)
- 5- year old boy with Weber-Christian Syndrome or histiocytic cytophagic panniculitis? Diagnostic difficulties. Case presentation
- A case of eosinophilic granuloma and its development to Hand-Schuller-Christian syndrome
- A case of Pfeifer-Weber-Christian syndrome
- A case of systemic Pfeiffer-Weber-Christian Syndrome complicated by DIC (author's transl)
- A case of Weber-Christian syndrome
- A special form of lupus disease. Deep cutaneous lupus. Apropos of 2 cases
- Acinar cell carcinoma of the pancreas revealed by Weber-Christian syndrome
- Acute pancreatitis and Weber-Christian syndrome
- Alpha-1-antitrypsin deficiency panniculitis
- Amyloidosis, Gaucher's disease, Hand-Schueller-Christian syndrome. Clinicodiagnostic viewpoint of metabolic diseases of the reticulohistiocytary system
- An etiologic and nosologic overview of craniosynostosis syndromes
- An unusual case which began with subcutaneous panniculitis followed by fever, severe hepatic involvement and hyperlipidemia
- Aural symptoms as primary presentation of Langerhan's cell histiocytosis
- Bone localization of Weber-Christian syndrome associated with chronic pancreatitis developing bone metastasis of pancreatic adenocarcinoma
- Case of association of Weber-Christian syndrome with bronchial asthma
- Case of extensive reticuloxanthomatosis (Hand-Schueller-Christian syndrome)
- Case of nodular non-suppurative paniculitis (Weber-Christian syndrome)
- Case of Weber-Christian syndrome
- Case of Weber-Christian syndrome in a 14-year-old girl
- Changes in serum enzymes in severe liver damage in Pfeifer-Weber-Christian syndrome with fatal outcome
- Chronic disseminated form of histiocytosis X (Hand-Schueller-Christian syndrome) in a 16-year-old boy
- Classification of the Hand-Schuller-Christian syndrome. With description of a recovered case (25-year follow-up) treated with cortisone
- Corticosteroid-sparing effect of hydroxychloroquine in a patient with early-onset Weber-Christian syndrome
- Disseminated histiocytosis X
- Endoscopic treatment of subcutaneous fat necrosis secondary to pancreatic-vascular fistula: apropos of a case
- Eosinophilic granuloma of bone
- Eosinophilic granuloma: resolution of lesion after biopsy
- Fatal course of a fungal pneumonia in glucocorticoid-treated recurrent febrile nodular panniculitis; Pfeifer-Weber-Christian syndrome
- Fatal panniculitis
- Hand Schuller Christian syndrome. Report of a case
- Hand-Schueller-Christian syndrome as a cause of chronic cor pulmonale
- Hand-Schueller-Christian syndrome in an infant
- Hand-Schuller-Christian syndrome
- Hand-Schuller-Christian syndrome arising in the mandible. A case report
- Hand-Schuller-Christian syndrome combined with empty sella syndrome: A case report and literature review
- Hand-Schuller-Christian syndrome with lung involvement
- Histiocytosis syndrome in children
- Histiocytosis X in dentistry: a propos of a case of Hand-Schuller-Christian syndrome
- Histiocytosis X of the ear and temporal bone: review of 22 cases
- Histiocytosis X. 2 cases of the Hand-Schueller-Christian syndrome
- Histiocytosis X. 3 different cases: eosinophilic granuloma, Hand-Schueller-Christian disease, Abt-Letterer-Siwe disease
- Idiopathic histiocytosis: a discussion of eosinophilic granuloma, the Hand-Schuller-Christian syndrome, and the Letterer-Siwe syndrome
- Imaging of Hand-Schuller-Christian syndrome by a monoclonal antibody
- Isolated ilial tuberculosis and its differential diagnosis
- Langerhans cell histiocytosis, diabetes insipidus, hyperprolactinemia and empty sella: a four-fold association. Report of two cases
- Langerhans cells histiocytosis in one family
- Langerhans-cell histiocytosis in twin sisters
- Maxillofacial manifestations of Langerhans cell histiocytosis: a clinical and therapeutic analysis of 10 patients
- Mitochondrial impairment and synaptic dysfunction are associated with neurological defects in iPSCs-derived cortical neurons of MERRF patients
- Morphology and pathogenesis of Pfeifer-Weber-Christian syndrome
- Multiple endocrine disorders in histiocytosis-X (Hand-Schueller-Christian syndrome)
- Narrowband ultraviolet B light in Langerhans cell histiocytosis: a case report
- Newly diagnosed ANCA-associated vasculitis after COVID-19 infection: a case report
- Observation of Pfeiffer-Weber-Christian syndrome, simulating sepsis
- Ocular pathology associated with the Weber Christian syndrome
- On 3 cases of Weber-Christian syndrome
- Oral manifestations of Lpngerhans' cell histiocytosis. Therapeutic strategies involving oral and maxillofacial surgery
- Overdose of vinblastine in a child with Langerhans' cell histiocytosis: toxicity and salvage therapy
- Pancreatic-portal fistula. A rare complication of chronic pancreatitis
- Panniculitis due to potassium bromide
- Panniculitis in children
- Peripheral facial paralysis in a case of chronic disseminated histiocytosis X (Hand-Schueller-Christian syndrome)
- Pfeifer-Weber-Christian syndrome and subacute pancreatitis. Apropos of a case
- Pfeifer-Weber-Christian syndrome associated with Kikuchi syndrome in infliximab therapy: development of necrotizing allergic vasculitis
- Pfeifer-Weber-Christian syndrome of the mesentery. Clinical and pathologico-anatomical aspects
- Pfeifer-Weber-Christian syndrome. Clinical and histological study of the ocular lesions
- Primary multinodular panniculitis or fat necrosis in children
- Prolonged remission of Weber-Christian syndrome in an infant
- Radiation treatment of Hand-Schueller-Christian syndrome in a child
- Rôle et organisation des unités transversales d’éducation thérapeutique du patient dans les CHU et les CHR de France
- Salivary diurnal glucocorticoid profiles in monozygotic twins with intra-twin birthweight-differences
- Solitary eosinophilic granuloma of the third metacarpal at pediatric age
- Subacute cytosteatonecrosis of pancreatic origin. Surgical problem in 5 cases (author's transl)
- Successful treatment of Weber-Christian panniculitis with cyclosporin-A
- Ten-year course of early-onset Weber-Christian syndrome with recurrent pneumonia: a suggestion for pathogenesis
- Treatment of a patient with severe lactic acidosis and multiple organ failure due to mitochondrial myopathy: A case report
- Urolithiasis and bladder neck disease in a child with Hand-Schueller-Christian syndrome
- Visceral necrotic granulomatous panniculitis and its possible localization in the skeleton and in the hematopoietic tissues, associated with pancytopenia. Relation to the Weber-Christian syndrome
- Weber Christian syndrome due to pancreaticomesenteric fistula secondary to acute alcoholic pancreatitis: treatment with pancreatic sphincterotomy alone
- Weber--Christian syndrome in infancy
- Weber-Christian syndrome
- Weber-Christian syndrome
- Weber-Christian syndrome after endoscopic retrograde pancreatography
- Weber-Christian syndrome and biliary-pancreatic cancer: 2 cases
- Weber-Christian syndrome and chronic pancreatitis (author's transl)
- Weber-Christian syndrome and chronic pancreatitis (author's transl)
- Weber-Christian syndrome and intraductal papillary mucinous tumor of the pancreas
- Weber-Christian syndrome and pancreatic cancer
- Weber-christian syndrome and pancreatic carcinoma. Report of a case and review of the literature (author's transl)
- Weber-Christian syndrome and pancreatic involvement. Apropos of a case with review of the literature
- Weber-Christian syndrome associated with an alpha-1 antitrypsin deficiency. Familial investigation
- Weber-Christian syndrome following endoscopic Wirsung duct radiography
- Weber-Christian syndrome in an 18-month-old infant
- Weber-Christian syndrome in pancreatic diseases
- Weber-Christian syndrome revealing intraductal papillary mucinous tumor of the pancreas
- Weber-Christian syndrome. Description of a case
- Weber-Christian syndrome. Description of a case with unusual onset and localization
- Xanthoma disseminatum. An unusual histiocytosis syndrome
- Xanthomatosis palpebro-cerebralis--clinical variants of the Hand-Schuller-Christian syndrome