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16 in total

1. Morphologic considerations on the placenta in congenital nephrotic syndrome of Finnish type.

Authors: C Inferrera; G Barresi; S Chimicata; F De Luca; G Baviera; V Gulli; M Gemelli
Journal: Virchows Arch A Pathol Anat Histol Date: 1980

2. Frequent relapser minimal change nephrosis: an unrecognized X-linked disorder?

Authors: N B Awadalla; A S Teebi; A Y Elzouki; A Shaltout
Journal: Eur J Pediatr Date: 1989-12 Impact factor: 3.183

3. Familial infantile nephrotic syndrome with ocular abnormalities.

Authors: C Glastre; P Cochat; R Bouvier; S Colon; X Cottin; D Giffon; C Wright; F Dijoud; L David
Journal: Pediatr Nephrol Date: 1990-07 Impact factor: 3.714

4. Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome.

Authors: B Z Garty; B Eisenstein; J Sandbank; S Kaffe; R Dagan; N Gadoth
Journal: J Med Genet Date: 1994-02 Impact factor: 6.318

5. The contribution of ultrasound for the differential diagnosis of congenital and infantile nephrotic syndrome.

Authors: Hanna Salame; Nash Damry; Katt Vandenhoudt; Michèle Hall; Fred E Avni
Journal: Eur Radiol Date: 2003-05-08 Impact factor: 5.315

6. Pathologic findings in adenosine deaminase-deficient severe combined immunodeficiency. I. Kidney, adrenal, and chondro-osseous tissue alterations.

Authors: H Ratech; M A Greco; G Gallo; D L Rimoin; H Kamino; R Hirschhorn
Journal: Am J Pathol Date: 1985-07 Impact factor: 4.307

[Heterogeneity of early onset nephrotic syndromes in infants (nephrotic syndrome "in infants"). Anatomical, clinical and genetic study of 37 cases].

1. Morphologic considerations on the placenta in congenital nephrotic syndrome of Finnish type.

2. Frequent relapser minimal change nephrosis: an unrecognized X-linked disorder?

3. Familial infantile nephrotic syndrome with ocular abnormalities.

4. Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome.

5. The contribution of ultrasound for the differential diagnosis of congenital and infantile nephrotic syndrome.

6. Pathologic findings in adenosine deaminase-deficient severe combined immunodeficiency. I. Kidney, adrenal, and chondro-osseous tissue alterations.

Review 7. Nephrotic syndrome in the 1st year of life.

8. A case of congenital nephrotic syndrome associated with positive C1q immunofluorescence.

9. Cortical microcystic disease of the kidney with dominant inheritance: a previously undescribed syndrome.

Review 10. Spontaneous remission of congenital nephrotic syndrome: a case report and review of the literature.