Literature DB >> 14207890

HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS.

H KOPELMAN, A M ASATOOR, M D MILNE.   

Abstract

Keywords:  AMINO ACID METABOLISM, INBORN ERRORS; BLOOD; BLOOD CHEMICAL ANALYSIS; CHROMATOGRAPHY; DISEASES IN TWINS; EXCRETION; GENETICS, HUMAN; GLYCINE; HYDROXYPROLINE; NEPHROTIC SYNDROME; PATHOLOGY; PROLINE; PROTEINURIA; URINE

Mesh：

Substances：

Year:  1964        PMID： 14207890     DOI： 10.1016/s0140-6736(64)92605-4

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


× No keyword cloud information.
  8 in total

1.  Set of simple side-room urine tests for detection of inborn errors of metabolism.

Authors:  N R Buist
Journal:  Br Med J       Date:  1968-06-22

2.  Anterior lenticonus and Alport's syndrome.

Authors:  E J Arnott; M D Crawfurd; P J Toghill
Journal:  Br J Ophthalmol       Date:  1966-07       Impact factor: 4.638

3.  Recurrent haematuria in childhood.

Authors: 
Journal:  Br Med J       Date:  1966-05-28

4.  The prognosis and management of renal tubular disorders.

Authors:  M D Milne
Journal:  Proc R Soc Med       Date:  1967-11-01

5.  Hyperprolinaemia type I and white matter disease: coincidence or causal relationship?

Authors:  M Steinlin; E Boltshauser; B Steinmann; W Wichmann; G Niemeyer
Journal:  Eur J Pediatr       Date:  1989-10       Impact factor: 3.183

6.  Familial glomerulopathy with giant fibrillar deposits.

Authors:  M Bürgin; E Hofmann; F W Reutter; B A Gürtler; L Matter; J Briner; F Gloor
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1980

7.  Hereditary nephropathy with hematuria (Alport's syndrome).

Authors:  A Chiricosta; S L Jindal; J Metuzals; B Koch
Journal:  Can Med Assoc J       Date:  1970-02-28       Impact factor: 8.262

8.  Biochemical and clinical features of hereditary hyperprolinemia.

Authors:  Hiroshi Mitsubuchi; Kimitoshi Nakamura; Shirou Matsumoto; Fumio Endo
Journal:  Pediatr Int       Date:  2014-08       Impact factor: 1.524
  8 in total

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