(Q40404426)

English

Diagnostic challenges in a child with familial hemophagocytic lymphohistiocytosis type 3 (FHLH3) presenting with fulminant neurological disease

scientific article published on 21 November 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Diagnostic challenges in a child with familial hemophagocytic lymphohistiocytosis type 3 (FHLH3) presenting with fulminant neurological disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

familial hemophagocytic lymphohistiocytosis

0 references

author name string

James D Weisfeld-Adams

1

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Yitzchak Frank

2

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Vinod Havalad

3

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Joanne M Hojsak

4

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Roberto Posada

5

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Shipra M Kaicker

6

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Birte Wistinghausen

7

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

publication date

21 November 2008

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Child's Nervous System

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Europe PubMed Central

PubMed publication ID

20 September 2017

25

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Europe PubMed Central

PubMed publication ID

20 September 2017

2

1 reference

Europe PubMed Central

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20 September 2017

153-159

1 reference

Europe PubMed Central

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20 September 2017

Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial haemophagocytic reticulosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe steroid-resistant post-infectious encephalomyelitis: general features and effects of IVIg

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hemophagocytic lymphohistiocytosis: how late can the onset be?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial and acquired hemophagocytic lymphohistiocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary necrotizing lymphocytic central nervous system vasculitis due to perforin deficiency in a four-year-old girl

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acute disseminated encephalomyelitis or multiple sclerosis: can the initial presentation help in establishing a correct diagnosis?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features and viral serologies in children with multiple sclerosis: a multinational observational study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pediatric visceral leishmaniasis in southern France

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective natural killer cell function in patients with hemophagocytic lymphohistiocytosis and in first degree relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence in Sweden and clinical features of familial hemophagocytic lymphohistiocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology, immunopathogenesis and management of pediatric central nervous system inflammatory demyelinating conditions

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel Munc13-4 mutations in children and young adult patients with haemophagocytic lymphohistiocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A teenage boy with late onset hemophagocytic lymphohistiocytosis with predominant neurologic disease and perforin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemophagocytic lymphohistiocytosis and other hemophagocytic disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A neurologic presentation of familial hemophagocytic lymphohistiocytosis which mimicked septic emboli to the brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unrelated donor hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variations of the perforin gene in patients with multiple sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of novel MUNC13-4 mutations in familial haemophagocytic lymphohistiocytosis and functional analysis of MUNC13-4-deficient cytotoxic T lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lymphohistiocytosis: a multi-factorial syndrome of macrophagic activation clinico-pathological study of 38 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal sibling cases of familial hemophagocytic lymphohistiocytosis (FHL) with MUNC13-4 mutations: case reports

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemophagocytic syndrome: A misleading complication of visceral leishmaniasis in children--a series of 12 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/19023578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00381-008-0744-Z

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

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