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22 subtopics

 

  • alpha 1-Antitrypsin Deficiency
  • Cartilage Diseases
  • Cellulitis
  • Collagen Diseases
  • Cutis Laxa
  • Dermatomyositis
  • Dupuytren's Contracture
  • Homocystinuria
  • Lupus Erythematosus, Cutaneous
  • Lupus Erythematosus, Systemic
  • Marfan Syndrome
  • Mixed Connective Tissue Disease
  • Mucinoses
  • Neoplasms, Connective Tissue
  • Noonan Syndrome
  • Osteopoikilosis
  • Panniculitis
  • Penile Induration
  • Pseudoxanthoma Elasticum
  • Rheumatic Diseases
  • Scleroderma, Localized
  • Scleroderma, Systemic

Connective Tissue DiseasesFollow by RSS 

You've reached a pubget topic page. Below are the latest papers on this topic, with subtopics on the left.

keywords > Skin and Connective Tissue Diseases > Connective Tissue Diseases

Latest papers

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

Prevalence of pinguecula and pterygium in patients with thyroid orbitopathy.

Assessment of endpoints in pulmonary arterial hypertension associated with connective tissue disease

Expanding possibilities in the treatment of patient groups with previously difficult-to-treat patients.

Connective tissue diseases after heavy exposure to silica: a report of nine cases in stonemasons.

[Capillaroscopy. Procedure and nomenclature]

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2).

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