Spectrum of disease associated with partial lipodystrophy: lessons from a trial cohort

Melvin, Audrey
Savage, David
Stears, Anna

August 2019

Purpose of review: Lipodystrophy syndromes have an estimated prevalence of 1.3–4.7 cases per millio...

A genome-wide linkage scan for familial partial lipodystrophy susceptibility genes in a German kindreds

Lanktree, M.
Robinson, J.
Creider, J.
Cao, H.
Carter, D.
Horsch, D.
Hegele, R.

August 2007

Background: In Dunnigan-type familial partial lipodystrophy (FPLD) patients are born with normal fat...

Clinical presentations, metabolic abnormalities and end-organ complications in patients with familial partial lipodystrophy

Akinci, B.
Onay, H.
Demir, T.
Savas-Erdeve, Ş.
Gen, R.
Simsir, I.Y.
Keskin, F.E.
Erturk, M.S.
Uzum, A.K.
Yaylalı, Güzin Fidan
Ozdemir, N.K.
Atik, T.
Ozen, S.
Yurekli, B.S.
Apaydin, T.
Altay, C.
Akinci, G.
Demir, L.
Comlekci, A.
Secil, M.
Oral, E.A.

January 2017

Objective Familial partial lipodystrophy (FPLD) is a rare genetic disorder characterized by partial ...

Spectrum of disease associated with partial lipodystrophy: lessons from a trial cohort

Meral, Rasimcan
Oral, Elif A.
Neidert, Adam H.
Ajluni, Nevin
Conjeevaram, Hari
Omary, M. Bishr
Innis, Jeffrey W.
Tayeh, Marwan K.
Thomas, Peedikayil E.
Rupani, Amit R.
Buggs-Saxton, Colleen
Horowitz, Jeffrey F.
Chenevert, Thomas L.
DiPaola, Frank
McKenna, Barbara
Buras, Eric
Brady, Graham F.

January 2017

ContextPartial lipodystrophy (PL) is associated with metabolic co-morbidities but may go undiagnosed...

A subset of patients with acquired partial lipodystrophy developing severe metabolic abnormalities

Arkan, Tugba
Erturk, Mehmet Sercan
Cavdar, Umit
Akinci, Gulcin
DEMİR, TEVFİK
MIHÇI, ERCAN
Saydam, Basak Ozgen
ALTAY, CANAN
YILDIRIM ŞİMŞİR, ILGIN
Sonmez, Melda
AKINCI, BARIŞ
SEÇİL, MUSTAFA
HEKİMSOY, ZELİHA
KULAKSIZOĞLU, MUSTAFA

April 2019

Purpose/Aim of the study: Acquired partial lipodystrophy (APL) is a rare disease characterized by se...

Familial partial lipodystrophy syndromes

Fernández-Pombo, Antía
Sánchez Iglesias, Sofía
Cobelo Gómez, Silvia
Hermida Ameijeiras, Álvaro
Araújo-Vilar, David

January 2021

Lipodystrophies are a heterogeneous group of rare conditions characterised by the loss of adipose ti...

ENDOCRINE RESEARCH

Saydam, BO

January 2019

Purpose/Aim of the study: Acquired partial lipodystrophy (APL) is a rare disease characterized by se...

Monogenic forms of lipodystrophic syndromes - diagnosis, detection, and practical management considerations from clinical cases

Vatier, Camille
Vantyghem, Marie-Christine
Storey, Caroline
Jéru, Isabelle
Christin-Maitre, Sophie
Fève, Bruno
Lascols, Olivier
Beltrand, Jacques
Carel, Jean-Claude
Vigouroux, Corinne
Bismuth, Elise

January 2019

International audienceBACKGROUND: Lipodystrophic syndromes are rare diseases of genetic or acquired ...

Clinical characteristics of patients with acquired partial lipodystrophy: a multicenter retrospective study

Magno, Silvia
Ceccarini, Giovanni
Corvillo, Fernando
Pelosini, Caterina
Gilio, Donatella
Paoli, Melania
Fornaciari, Silvia
Pandolfo, Giuseppe
Sánchez Iglesias, Sofía
Nozal, Pilar
Curcio, Michele
Sessa, María Rita
López Trascasa, Margarita
Araújo-Vilar, David
Santini, Ferruccio

November 2023

Background Barraquer-Simons syndrome (BSS) is a rare, acquired form of lipodystrophy characterized ...

Diagnosis and treatment of lipodystrophy: a step-by-step approach

Araújo-Vilar, D
Santini, F

January 2019

Lipodystrophy syndromes are rare heterogeneous disorders characterized by deficiency of adipose tiss...

Microvascular complications in type 1 Diabetes: a comparative analysis of patients treated with autologous nonmyeloablative hematopoietic stem-cell transplantation and conventional medical therapy

Penaforte-Saboia, Jaquellyne G.
Montenegro Jr., Renan M.
Couri, Carlos E.
Batista, Livia A.
Montenegro, Ana Paula D. R.
Fernandes, Virginia O.
Akhtar, Hussain
Negrato, Carlos A.
Malmegrim, Kelen Cristina Ribeiro
Moraes, Daniela Aparecida
Dias, Juliana B. E.
Simões, Belinda P. S
Gomes, Marilia Brito
Oliveira, Maria Carolina

November 2017

Background: Dunnigan-type familial partial lipodystrophy (FPLD2) is a rare autosomal dominant diseas...

Acquired partial lipodystrophy is associated with increased risk for developing metabolic abnormalities

Akinci B.
Koseoglu F.D.
Onay H.
Yavuz S.
Altay C.
Simsir I.Y.
Ozisik S.
Demir L.
Korkut M.
Yilmaz N.
Ozen S.
Akinci G.
Atik T.
Calan M.
Secil M.
Comlekci A.
Demir T.

January 2015

PubMed ID: 26139569Objective Acquired partial lipodystrophy (APL) is a rare disorder characterized b...

Deciphering the Clinical Presentations in LMNA-related Lipodystrophy: Report of 115 Cases and a Systematic Review

Demir, KORCAN
Besci, Ozge
Foss de Freitas, Maria Christina
Guidorizzi, Natália Rossin
Guler, Merve Celik
Gilio, Donatella
Maung, Jessica N
Schill, Rebecca L
Hoose, Keegan S
Obua, Bonje N
Gomes, Anabela D
Şimşir, Ilgın Yıldırım
Akinci, Baris
MacDougald, Ormond A
Oral, Elif A

October 2023

Context: Lipodystrophy syndromes are a heterogeneous group of rare genetic or acquired disorders cha...

Partial lipodystrophy of the limbs in a diabetes clinic setting

Demir, Tevfik
Akinci, Baris
Demir, Leyla
Altay, Canan
Atik, Tahir
Cavdar, Umit
Secil, Mustafa
Comlekci, Abdurrahman

January 2016

WOS: 000380079700009PubMed ID: 26776282Objective: Partial lipodystrophy of the limbs (PLL) is a newl...

Metabolic Studies in Three Patients

October 2016

Metabolic studies were performed in three patients with partial lipodystrophy. These studies demonst...

Recent developments in Lipodystrophy

Melvin, Audrey
Savage, David
Stears, Anna

August 2019

Purpose of review: Lipodystrophy syndromes have an estimated prevalence of 1.3–4.7 cases per millio...

A genome-wide linkage scan for familial partial lipodystrophy susceptibility genes in a German kindreds

Lanktree, M.
Robinson, J.
Creider, J.
Cao, H.
Carter, D.
Horsch, D.
Hegele, R.

August 2007

Background: In Dunnigan-type familial partial lipodystrophy (FPLD) patients are born with normal fat...

Clinical presentations, metabolic abnormalities and end-organ complications in patients with familial partial lipodystrophy

Akinci, B.
Onay, H.
Demir, T.
Savas-Erdeve, Ş.
Gen, R.
Simsir, I.Y.
Keskin, F.E.
Erturk, M.S.
Uzum, A.K.
Yaylalı, Güzin Fidan
Ozdemir, N.K.
Atik, T.
Ozen, S.
Yurekli, B.S.
Apaydin, T.
Altay, C.
Akinci, G.
Demir, L.
Comlekci, A.
Secil, M.
Oral, E.A.

January 2017

Objective Familial partial lipodystrophy (FPLD) is a rare genetic disorder characterized by partial ...

Spectrum of disease associated with partial lipodystrophy: lessons from a trial cohort

Meral, Rasimcan
Oral, Elif A.
Neidert, Adam H.
Ajluni, Nevin
Conjeevaram, Hari
Omary, M. Bishr
Innis, Jeffrey W.
Tayeh, Marwan K.
Thomas, Peedikayil E.
Rupani, Amit R.
Buggs-Saxton, Colleen
Horowitz, Jeffrey F.
Chenevert, Thomas L.
DiPaola, Frank
McKenna, Barbara
Buras, Eric
Brady, Graham F.

January 2017

ContextPartial lipodystrophy (PL) is associated with metabolic co-morbidities but may go undiagnosed...

A subset of patients with acquired partial lipodystrophy developing severe metabolic abnormalities

Arkan, Tugba
Erturk, Mehmet Sercan
Cavdar, Umit
Akinci, Gulcin
DEMİR, TEVFİK
MIHÇI, ERCAN
Saydam, Basak Ozgen
ALTAY, CANAN
YILDIRIM ŞİMŞİR, ILGIN
Sonmez, Melda
AKINCI, BARIŞ
SEÇİL, MUSTAFA
HEKİMSOY, ZELİHA
KULAKSIZOĞLU, MUSTAFA

April 2019

Purpose/Aim of the study: Acquired partial lipodystrophy (APL) is a rare disease characterized by se...

Familial partial lipodystrophy syndromes

Fernández-Pombo, Antía
Sánchez Iglesias, Sofía
Cobelo Gómez, Silvia
Hermida Ameijeiras, Álvaro
Araújo-Vilar, David

January 2021

Lipodystrophies are a heterogeneous group of rare conditions characterised by the loss of adipose ti...

ENDOCRINE RESEARCH

Saydam, BO

January 2019

Purpose/Aim of the study: Acquired partial lipodystrophy (APL) is a rare disease characterized by se...

Monogenic forms of lipodystrophic syndromes - diagnosis, detection, and practical management considerations from clinical cases

Vatier, Camille
Vantyghem, Marie-Christine
Storey, Caroline
Jéru, Isabelle
Christin-Maitre, Sophie
Fève, Bruno
Lascols, Olivier
Beltrand, Jacques
Carel, Jean-Claude
Vigouroux, Corinne
Bismuth, Elise

January 2019

International audienceBACKGROUND: Lipodystrophic syndromes are rare diseases of genetic or acquired ...

Clinical characteristics of patients with acquired partial lipodystrophy: a multicenter retrospective study

Magno, Silvia
Ceccarini, Giovanni
Corvillo, Fernando
Pelosini, Caterina
Gilio, Donatella
Paoli, Melania
Fornaciari, Silvia
Pandolfo, Giuseppe
Sánchez Iglesias, Sofía
Nozal, Pilar
Curcio, Michele
Sessa, María Rita
López Trascasa, Margarita
Araújo-Vilar, David
Santini, Ferruccio

November 2023

Background Barraquer-Simons syndrome (BSS) is a rare, acquired form of lipodystrophy characterized ...

Diagnosis and treatment of lipodystrophy: a step-by-step approach

Araújo-Vilar, D
Santini, F

January 2019

Lipodystrophy syndromes are rare heterogeneous disorders characterized by deficiency of adipose tiss...

Microvascular complications in type 1 Diabetes: a comparative analysis of patients treated with autologous nonmyeloablative hematopoietic stem-cell transplantation and conventional medical therapy

Penaforte-Saboia, Jaquellyne G.
Montenegro Jr., Renan M.
Couri, Carlos E.
Batista, Livia A.
Montenegro, Ana Paula D. R.
Fernandes, Virginia O.
Akhtar, Hussain
Negrato, Carlos A.
Malmegrim, Kelen Cristina Ribeiro
Moraes, Daniela Aparecida
Dias, Juliana B. E.
Simões, Belinda P. S
Gomes, Marilia Brito
Oliveira, Maria Carolina

November 2017

Background: Dunnigan-type familial partial lipodystrophy (FPLD2) is a rare autosomal dominant diseas...

Acquired partial lipodystrophy is associated with increased risk for developing metabolic abnormalities

Akinci B.
Koseoglu F.D.
Onay H.
Yavuz S.
Altay C.
Simsir I.Y.
Ozisik S.
Demir L.
Korkut M.
Yilmaz N.
Ozen S.
Akinci G.
Atik T.
Calan M.
Secil M.
Comlekci A.
Demir T.

January 2015

PubMed ID: 26139569Objective Acquired partial lipodystrophy (APL) is a rare disorder characterized b...

Deciphering the Clinical Presentations in LMNA-related Lipodystrophy: Report of 115 Cases and a Systematic Review

Demir, KORCAN
Besci, Ozge
Foss de Freitas, Maria Christina
Guidorizzi, Natália Rossin
Guler, Merve Celik
Gilio, Donatella
Maung, Jessica N
Schill, Rebecca L
Hoose, Keegan S
Obua, Bonje N
Gomes, Anabela D
Şimşir, Ilgın Yıldırım
Akinci, Baris
MacDougald, Ormond A
Oral, Elif A

October 2023

Context: Lipodystrophy syndromes are a heterogeneous group of rare genetic or acquired disorders cha...

Partial lipodystrophy of the limbs in a diabetes clinic setting

Demir, Tevfik
Akinci, Baris
Demir, Leyla
Altay, Canan
Atik, Tahir
Cavdar, Umit
Secil, Mustafa
Comlekci, Abdurrahman

January 2016

WOS: 000380079700009PubMed ID: 26776282Objective: Partial lipodystrophy of the limbs (PLL) is a newl...

Metabolic Studies in Three Patients

October 2016

Metabolic studies were performed in three patients with partial lipodystrophy. These studies demonst...

Recent developments in Lipodystrophy

Melvin, Audrey
Savage, David
Stears, Anna

August 2019

Purpose of review: Lipodystrophy syndromes have an estimated prevalence of 1.3–4.7 cases per millio...

A genome-wide linkage scan for familial partial lipodystrophy susceptibility genes in a German kindreds

Lanktree, M.
Robinson, J.
Creider, J.
Cao, H.
Carter, D.
Horsch, D.
Hegele, R.

August 2007

Background: In Dunnigan-type familial partial lipodystrophy (FPLD) patients are born with normal fat...

Clinical presentations, metabolic abnormalities and end-organ complications in patients with familial partial lipodystrophy

Akinci, B.
Onay, H.
Demir, T.
Savas-Erdeve, Ş.
Gen, R.
Simsir, I.Y.
Keskin, F.E.
Erturk, M.S.
Uzum, A.K.
Yaylalı, Güzin Fidan
Ozdemir, N.K.
Atik, T.
Ozen, S.
Yurekli, B.S.
Apaydin, T.
Altay, C.
Akinci, G.
Demir, L.
Comlekci, A.
Secil, M.
Oral, E.A.

January 2017

Objective Familial partial lipodystrophy (FPLD) is a rare genetic disorder characterized by partial ...

Spectrum of disease associated with partial lipodystrophy: lessons from a trial cohort

Abstract

Extracted data

Spectrum of disease associated with partial lipodystrophy: lessons from a trial cohort

Abstract

Extracted data

Related items

Related items